Reproductive ablation constructs

ABSTRACT

The present invention relates to the regulation of reproductive development, particularly to the genetic ablation of reproductive tissues in angiosperm and gymnosperm species. Reproductive-preferred promoters, regulatory elements, and cytotoxic nucleotide sequences are disclosed herein, as are constructs and methods for genetic ablation.

FIELD OF INVENTION

The present invention relates to the regulation of reproductive development. In particular, this invention relates to the genetic ablation of reproductive tissues in angiosperm and gymnosperm species. Reproductive-preferred promoters, regulatory elements, and cytotoxic nucleotide sequences are provided. Constructs and methods for genetic ablation are also included in the invention.

BACKGROUND OF THE INVENTION

With the advent of plant genetic engineering technology, the ecological implications of genetically modified crops are of great concern, particularly when there are no inherent barriers to the spread of transgenes through sexual reproduction. Specifically, concerns have arisen in cases when transgenes can spread from a transgenic plant to a weedy species through hybridization, or when the crop species itself exists in weedy forms. Bergelson et al. Nature 395: 25 (1998). One way to address such concerns is by genetically engineering sterility in a plant through complete ablation of reproductive structures.

Recently, there has been significant interest in using an ablation system for controlling reproductive development in plants. Reproductive control has been achieved in several plant species by genetic ablation, which entails linking a reproductive-preferred promoter with a cytotoxic gene to ablate reproductive cells. For example, barnase, an extracellular ribonuclease from Bacillus amyloliquifaciens has been employed for inducing male sterility. Paddon et al. J. Bacteriol. 171:1185-1187 (1989). European Patent No. 344,029 describes a system for producing a male sterile plant by transforming a plant with a DNA encoding barnase under the control of a tapetum-specific promoter. Transformation of tobacco and oilseed rape plants with such a promoter-gene construct prevented the plants from producing fertile pollen. Mariani et al., Nature 347: 737-741 (1990). Flowers of transgenic Arabidopsis thaliana plants expressing a fusion construct of the APETALA3 (AP3) promoter and the diphtheria toxin A chain (DTA) gene lack petals and stamens, suggesting that transgene expression ablated petal and stamen cells. Transgenic Arabidopsis expressing the DTA gene under control of the LEAFY promoter produced no flowers. Tobacco plants transformed with a tobacco stigma-specific promoter driving the barnase gene lacked the stigmatic secretory zone and were female sterile.

Although genetic ablation has been effective, the promoters generally used for ablation are not well-suited for tissue-specific expression. As a consequence, leaky gene expression can significantly reduce and damage plant vegetative growth. Depending on the plant species, ablation can reduce vegetative growth by 80%. Strauss, S. H. and Meilan, R. TGERC Annual Report (1998). For genetic ablation to be commercially useful in the forestry industry, the amount of damage to vegetative tissues must be minimized to nominal levels.

While numerous patents and patent application publications disclose genetic ablation using a variety of promoters and cytotoxic genes, there is little disclosure addressing the effects of ablation on a plant's vegetative growth and development. The LFY promoter from Arabidopsis, which is expressed strongly in floral meristems and weakly in developing leaves, has been used for producing plants with ablated flowers. Nilsson et al., Plant J. 15:799-804 (1998). However, very few plants transformed with LFY had ablated flowers and uncompromised vegetative development. Therefore, it would be impractical to use a similar approach for reproductive ablation in a tree species, since it would take years to produce, grow, and test many transgenic trees to identify those few trees that have sterility and normal vegetative growth.

The genetic ablation of a reproductive organ requires a delicate balance between promoter activity and ablation gene toxicity. While the barnase gene is widely used for ablation in plants, barnase-induced toxicity frequently causes detrimental effects on plant growth and development. Thus, it may be desirable to reduce the toxicity of barnase, such that reproductive ablation occurs without deleterious and unrecoverable damages to a plant's vegetative growth.

Concurrent with the production of a mutant barnase having reduced toxicity, it may also be desirable to minimize leaky expression of a reproductive ablation construct in a plant's vegetative tissues. By minimizing leaky or ectopic expression of a reproductive ablation construct in a plant, expression of a mutant barnase gene in the vegetative tissues may be better tolerated by the plant due to attenuated ablation, which depends on promoter activity and RNase activity of a barnase mutant.

Accordingly, there exists a need for a reproductive ablation system having reduced barnase-induced toxicity and minimal leaky expression in a plant's vegetative tissues.

SUMMARY OF THE INVENTION

The present invention provides an isolated polynucleotide selected from the group consisting of SEQ ID NOs: 1-8 and 13-17, as well as a plasmid comprising the sequence depicted in any one of SEQ ID NOs. 18-27.

The present invention also provides a plasmid comprising the sequence depicted in any one of FIG. 1 (i.e., SEQ ID NO. 18), FIG. 2 (i.e., SEQ ID NO. 19), FIG. 3 (i.e., SEQ ID NO. 20), FIG. 4 (i.e., SEQ ID NO. 21), FIG. 5 (i.e., SEQ ID NO. 22), FIG. 6 (i.e., SEQ ID NO. 23), FIG. 7 (i.e., SEQ ID NO. 24), FIG. 8 (i.e., SEQ ID NO. 25), FIG. 9 (i.e., SEQ ID NO. 26), or FIG. 19 (i.e., SEQ ID NO. 27).

Also provided is an isolated polynucleotide that confers reproductive-preferred gene expression in a plant cell, wherein the polynucleotide comprises the sequence depicted in any one of SEQ ID NOs. 1, 2, 3, 4, or 16.

In one embodiment, the polynucleotide confers male-preferred gene expression in a plant cell.

Also provided is a promoter comprising the sequence depicted in any one of SEQ ID NOs. 1, 2, 3, 4, or 16.

In one embodiment, the polynucleotide of SEQ ID NOs. 1-8 is expressed or is active in a pre-male or pre-female reproductive structure.

Also provided is an isolated polynucleotide that has a sequence identity that is greater than or equal to 99%, 98%, 97%, 96%, 95%, 94%, 93%, 92%, 91%, 90%, 89%, 88%, 87%, 86%, 85%, 84%, 83%, 82%, 81%, 80%, 79%, 78%, 77%, 76%, 75%, 74%, 73%, 72%, 71%, 70%, 69%, 68%, 67%, 66%, 65%, 64%, 63%, 62%, 61%, or 60% in sequence to any one of SEQ ID NOs: 1, 2, 3, 4, or 16.

In another embodiment, a polynucleotide is provided that has a sequence selected from the group consisting of (i) sequences that are complementary to a polynucleotide of any one of SEQ ID NOs. 1-8 and 16-17, (ii) sequences that are reverse sequences of a polynucleotide of any one of SEQ ID NOs. 1-8 and 16-17, and (iii) sequences that are reverse complements of a polynucleotide of any one of SEQ ID NOs. 1-8 and 16-17.

Also provided is an isolated polynucleotide that hybridizes under stringent conditions to a polynucleotide of claim 1, wherein said isolated polynucleotide hybridizes over its full-length sequence to a polynucleotide of any of one of SEQ ID NOs. 1-26.

Also provided is an isolated polynucleotide comprising the sequence depicted in SEQ ID NO. 17.

In one embodiment, a polynucleotide is provided that has the sequence of any one of SEQ ID NOs. 1-4 and 16 which is capable of at least one of (i) binding to a nucleic acid molecule or (ii) regulating expression of an operably-linked gene in a dicotyledonous plant.

In another embodiment, a polynucleotide is provided that has the sequence of any one of SEQ ID NOs. 1-4 and 16 which is capable of at least one of (i) binding to a nucleic acid molecule or (ii) regulating expression of an operably-linked gene in a gymnosperm.

In one embodiment, a polynucleotide is provided that has the sequence of any one of SEQ ID NOs. 1-4 and 16 which is capable of upregulating or downregulating the expression of an operably-linked gene in a plant.

In one aspect of the present invention, a construct is provided that comprises an isolated polynucleotide selected from any one of SEQ ID NO: 1, 2, 3, 4, or 16 and functional variants thereof operably linked to a desired nucleic acid, wherein said promoter regulates the expression of said desired nucleic acid in a plant cell transformed with the construct. In one embodiment, the polynucleotide upregulates or downregulates expression of said desired nucleic acid. In another embodiment, the desired nucleic acid encodes an expression product that is capable of disrupting reproductive development in a plant.

The present invention provides a plant transformed with any of the constructs disclosed herein. In one embodiment, the phenotype of such a transformed plant expresses a difference in reproductive development compared with a plant of the same species that is not transformed with said construct. In one embodiment, the difference in reproductive development occurs in a male reproductive structure. In another embodiment, the difference in reproductive development occurs in any one of anther, filament, tapetum, pollen, microsporophyll, or staminate cone. In an alternative embodiment, the difference in reproductive development occurs in a female reproductive structure. In that case, in one embodiment, the difference in reproductive development occurs in any one of stigma, style, ovary, megaspore, ovuliferous cone. In yet another embodiment, the difference in reproductive development occurs in a pre-male or pre-female reproductive structure.

In one aspect, a desired nucleic acid may produce an RNA transcript, which, in one embodiment, may comprise an antisense sequence of a gene that is endogenous to the plant cell. In one embodiment, the RNA transcript induces RNA interference of a gene that is normally expressed in the plant cell.

Also provided is a plant cell comprising a construct comprising (i) a polynucleotide having the sequence of any one of SEQ ID NOs: 1, 2, 3, 4, or 16 or functional variants thereof and (ii) a desired nucleic acid, wherein said polynucleotide is operably linked to said desired nucleic acid. A transgenic plant comprising such a plant cell is also provided.

In one aspect, the present invention provides a method for producing a transgenic plant, comprising (a) transforming a plant cell with a construct that comprises (i) at least one polynucleotide having the sequence of any one of SEQ ID NOs. 1, 2, 3, 4, or 16 or functional variants thereof and (ii) a desired nucleic acid, wherein said polynucleotide regulates the activity of said desired sequence; (b) culturing said transformed plant cell under conditions that promote growth of a plant, wherein said plant is a transgenic plant that exhibits a phenotype that is different from a plant of the same species that does not contain said construct.

In one embodiment, the phenotype of the transformed plant is characterized by a difference in reproductive development compared with a plant of the same species that does not contain the construct. In another embodiment, the phenotype of the transformed plant is characterized by a difference in male reproductive development compared with a plant of the same species that does not contain the construct. Alternatively, the phenotype of the transformed plant is characterized by a difference in female reproductive development compared with a plant of the same species that does not contain the construct. In yet another embodiment, the phenotype of the transformed plant is characterized by a difference in a pre-male or pre-female reproductive structure compared with a plant of the same species that does not contain the construct.

In another aspect, a method for conferring reproductive sterility in a plant is provided, comprising (a) introducing into a plant cell a construct comprising (i) a promoter having the sequence of any one of SEQ ID NOs: 1, 2, 3, 4, or 16 or functional variants thereof and (ii) a nucleic acid encoding a gene that is capable of ablating reproductive development, wherein said nucleic acid is sense relative to said promoter and wherein said promoter regulates the expression of said gene; (b) culturing said transformed plant cell under conditions that promote growth of a plant, wherein said plant is a transgenic plant that exhibits a phenotype that is different from a plant of the same species that does not contain said construct; and (c) selecting a plant that is reproductive-sterile.

In another aspect is a method for ablating a reproductive structure in a plant, comprising (a) introducing into a plant cell a construct comprising (i) a promoter having the sequence of any one of SEQ ID NOs: 1, 2, 3, 4, or 16 or functional variants thereof and (ii) a nucleic acid encoding a gene that is capable of ablating reproductive development, wherein said promoter regulates the expression of said gene; (b) culturing said transformed plant cell under conditions that promote growth of a plant, wherein said plant is a transgenic plant that exhibits a phenotype that is different from a plant of the same species that does not contain said construct; and (c) selecting a plant having an ablated reproductive structure. In one embodiment, the plant is selected from an angiosperm or gymnosperm species.

Also provided is a method for altering pollen fertility, comprising (a) introducing into a plant cell of a woody plant a construct comprising (i) a promoter having the sequence of any one of SEQ ID NOs: 1, 2, 3, 4, or 16 or functional variants thereof and (ii) and a desired nucleic acid, wherein said promoter regulates the expression of said desired nucleic acid; (b) culturing said transformed plant cell under conditions that promote growth of a plant; and (c) obtaining a plant having altered pollen fertility. In one embodiment, the woody plant is selected from a species of Eucalyptus or Pinus.

Also provided herein is an isolated polynucleotide selected from any one of SEQ ID NO: 5-8 and variants thereof. In one embodiment, any one of these polynucleotides encods a mutant barnase enzyme. In one embodiment, such a polynucleotide encodes a mutant barnase enzyme having attenuated activity compared with a wild-type barnase enzyme. In one embodiment, the variant has a sequence identity that is greater than or equal to 99%, 98%, 97%, 96%, 95%, 94%, 93%, 92%, 91%, 90%, 89%, 88%, 87%, 86%, 85%, 84%, 83%, 82%, 81%, 80%, 79%, 78%, 77%, 76%, 75%, 74%, 73%, 72%, 71%, 70%, 69%, 68%, 67%, 66%, 65%, 64%, 63%, 62%, 61%, or 60% in sequence to any one of SEQ ID NOs: 5-8.

Also provided is an isolated polynucleotide having a sequence selected from (i) sequences that are complementary to a polynucleotide of any one of SEQ ID NOs: 5-8, (ii) sequences that are reverse sequences of a polynucleotide of any one of SEQ ID NOs: 5-8, and (iii) sequences that are reverse complements of a polynucleotide of any one of SEQ ID NOs: 5-8.

In another embodiment, an isolated polynucleotide that hybridizes under stringent conditions to a polynucleotide of any one of SEQ ID NOs: 5-8, wherein the isolated polynucleotide hybridizes over its full-length sequence to a polynucleotide of any one of SEQ ID NO: 5-8.

In another aspect, a method for conferring reproductive sterility in a plant without disturbing vegetative growth is provided, comprising (a) introducing into a plant cell a construct comprising (i) a promoter having reproductive-preferred activity; (ii) a nucleic acid encoding a gene that is capable of ablating reproductive development, wherein said promoter regulates the expression of said gene; (b) culturing said transformed plant cell under conditions that promote growth of a plant, wherein said plant is a transgenic plant that exhibits a phenotype that is different from a plant of the same species that does not contain said construct; and (c) selecting a plant having reproductive-sterility and undisturbed vegetative growth.

Also provided is a method for ablating reproductive development in a plant without disturbing vegetative growth, comprising (a) introducing into a plant cell a construct comprising (i) a promoter having the sequence of any one of SEQ ID NOs: 1, 2, 3, 4, or 16 or functional variants thereof, (ii) a nucleic acid encoding a gene that is capable of ablating reproductive development, wherein said promoter regulates the expression of said gene; (b) culturing said transformed plant cell under conditions that promote growth of a plant, wherein said plant is a transgenic plant that exhibits a phenotype that is different from a plant of the same species that does not contain said construct; and (c) selecting a plant having ablated reproductive development and undisturbed vegetative growth.

Also provided is a method for conferring male-sterility in a plant without disturbing vegetative growth, comprising (a) introducing into a plant cell a construct comprising (i) a promoter having reproductive-preferred expression; (ii) a nucleic acid encoding a mutant barnase, wherein said mutant barnase has attenuated activity compared with wild-type barnase; (b) culturing said transformed plant cell under conditions that promote growth of a plant, wherein said plant is a transgenic plant that exhibits a reproductive phenotype that is different from a plant of the same species that does not contain said construct; and (c) selecting a plant having male-sterility and undisturbed vegetative growth. In one embodiment, the promoter has a sequence selected from the group consisting of SEQ ID NOs: 1, 2, 3, 4, and 16. In another embodiment, the promoter is a functional variant of any one of the sequences selected from the group consisting of SEQ ID NOs: 1, 2, 3, 4, and 16.

In one embodiment, the nucleic acid of (ii) above has the sequence of any of one of SEQ ID NOs: 5-8.

The present invention also provides in one embodiment, a plant having ablated reproductive development and unaffected vegetative growth.

The present invention also provides in another embodiment, a woody plant having ablated reproductive development and normal vegetative growth.

In a further aspect, a method for obtaining wood is provided, comprising (a) introducing into a plant cell of a woody plant a construct comprising (i) a promoter having the sequence of any one of SEQ ID NOs: 1, 2, 3, 4, or 16 or functional variants thereof and (ii) and a desired nucleic acid, wherein said promoter regulates the expression of said desired nucleic acid; (b) culturing said transformed plant cell under conditions that promote growth of a plant; and (c) obtaining wood from said plant.

In another aspect is a method for obtaining wood pulp, comprising (a) introducing into a plant cell of a woody plant a construct comprising (i) a promoter having the sequence of any one of SEQ ID NOs: 1, 2, 3, 4, or 16 or functional variants thereof and (ii) and a desired nucleic acid, wherein said promoter regulates the expression of said desired nucleic acid; (b) culturing said transformed plant cell under conditions that promote growth of a plant; and (c) obtaining wood pulp from said plant.

Also provided is a method for ablating a reproductive structure in a plant, comprising (a) introducing into a plant cell a plasmid selected from the group consisting of SEQ ID NO 13-15; (b) culturing said transformed plant cell under conditions that promote growth of a plant, wherein said plant is a transgenic plant that exhibits a phenotype that is different from a plant of the same species that does not contain said plasmid; and (c) selecting a plant having an ablated reproductive structure. In another embodiment, a plasmid selected from the group consisting of SEQ ID NO 18-26 may be introduced into the plant cell in step (a) above.

Also provided is a method for conferring reproductive sterility in a plant, comprising (a) introducing into a plant cell a plasmid selected from the group consisting of SEQ ID NO 13-15; (b) culturing said transformed plant cell under conditions that promote growth of a plant, wherein said plant is a transgenic plant that exhibits a phenotype that is different from a plant of the same species that does not contain said plasmid; and (c) selecting a plant having an ablated reproductive structure. In another embodiment, a plasmid selected from the group consisting of SEQ ID NO 18-26 may be introduced into the plant cell in step (a) above.

In another embodiment, a plant is provided that is stably transformed with any of the plasmids disclosed herein. In one embodiment the plasmid that is stably introduced into the plant has the sequence of any one of SEQ ID NOs. 13-15 or 18-26.

The present invention also provides a method for conferring reproductive sterility in a transgenic plant, comprising (a) transforming a plant cell with a construct having a reproductive-preferred promoter operably linked to a cytotoxic gene and a non-reproductive-preferred promoter operably linked to a gene encoding a protein that inhibits said cytotoxic gene; wherein said reproductive-preferred promoter is active in an angiosperm or gymnosperm reproductive structure and said non-reproductive-preferred promoter is not active in an angiosperm or gymnosperm reproductive structure; (b) culturing said transformed plant cell under conditions that promote growth of a plant; and (c) selecting a transgenic plant having an ablated reproductive structure. In one embodiment, the reproductive-preferred promoters are selected from the group consisting of SEQ ID NOs: 1, 2, 3, 4, or 16. In another embodiment, the non-reproductive-preferred promoters are selected from the group consisting of SEQ ID NO: 3 and SEQ ID NO. 17.

Also provided is a polypeptide comprising the amino acid sequence depicted in any one of SEQ ID NOs.: 9-12 or variant thereof. In one embodiment, the variant of the polypeptide has a sequence identity that is greater than or equal to 99%, 98%, 97%, 96%, 95%, 94%, 93%, 92%, 91%, 90%, 89%, 88%, 87%, 86%, 85%, 84%, 83%, 82%, 81%, 80%, 79%, 78%, 77%, 76%, 75%, 74%, 73%, 72%, 71%, 70%, 69%, 68%, 67%, 66%, 65%, 64%, 63%, 62%, 61%, or 60% in sequence to any one of SEQ ID NOs: 9-12.

The present invention also contemplates a construct, comprising a promoter comprising the sequence of either of SEQ ID NOs. 1 or 2 operably linked to a polynucleotide comprising the sequence of any one of SEQ ID NOs 5-8. In one embodiment, the polynucleotide comprises the sequence depicted in SEQ ID NO. 5. In one embodiment, the polynucleotide comprises the sequence depicted in SEQ ID NO. 6. In another embodiment, the polynucleotide comprises the sequence depicted in SEQ ID NO. 7. In another embodiment, the polynucleotide comprises the sequence depicted in SEQ ID NO. 8. Also provided is a plant transformed with this construct.

Also provided is a construct comprising a promoter comprising the sequence of either of SEQ ID NOs. 1 or 2 operably linked to a polynucleotide that encodes a polypeptide comprising the amino acid sequence depicted in any one of SEQ ID NOs. 9-12. Also provided is a plant transformed with this construct.

In one embodiment, one of these constructs may also comprise a non-reproductive preferred promoter operably linked to a barstar gene.

The non-reproductive preferred promoter disclosed herein may comprise the sequence depicted in SEQ ID NO. 3 or SEQ ID NO. 17.

Also provided is a method of inducing formation of strobili in Pinus comprising (a) obtaining a hybrid progeny plant from the cross of pitch pine P. rigida with a loblolly pine P. taeda, (b) transforming the hybrid plant with a desired polynucleotide that is operably linked to a reproductive tissue preferred promoter, (c) regenerating a transgenic hybrid plant from the transformed hybrid plant, and (d) recovering strobili. In one embodiment, the reproductive tissue preferred promoter comprises the sequence depicted in any one of SEQ ID NOs. 1, 2, 3, 4, or 16. In another embodiment, the hybrid plant is transformed by Agrobacterium or biolistics-mediated transformation. In one embodiment, the strobili are male or female. In another embodiment, the strobili are produced by the transgenic hybrid plant within 1-3 years of transformation.

In another aspect, a method of testing a candidate promoter for activity in a gymnosperm reproductive tissue is provided, comprising (a) obtaining a candidate promoter sequence, (b) operably linking the candidate promoter to a reporter gene, (c) introducing the candidate promoter that is operably linked to the reporter gene into a plant material, and (d) identifying expression of the reporter gene in the plant material. In this method, the reporter gene is GUS. In one embodiment, the plant material is a plant explant or plant cell. In another embodiment, the plant material in which the reporter gene expression is identified is selected from the group consisting of petals, stamens, carpels, shoot tips, anthers, tapetum, callus, and embryo.

The present invention also provides a hybrid progeny plant, comprising a reproductive tissue preferred promoter operably linked to a desired polynucleotide, wherein the hybrid progeny plant is obtained from the cross of pitch pine P. rigida with loblolly pine P. taeda. In one embodiment, the reproductive tissue preferred promoter comprises the sequence depicted in any one of SEQ ID NOs. 1, 2, 3, 4, or 16. In one embodiment, the desired polynucleotide comprises the sequence depicted in any one of SEQ ID NOs. 5-8. In another embodiment, the desired polynucleotide encodes a polypeptide that comprises the amino acid sequence depicted in any one of SEQ ID NOs. 9-12. Also provided is a hybrid progeny plant transformed with a construct comprising the sequence of any of SEQ ID NOs. 13-15, wherein the hybrid progeny plant is obtained from the cross of pitch pine P. rigida with loblolly pine P. taeda.

The present invention also provides a method of testing putative flowering control constructs for activity in delaying reproduction in gymnosperms, comprising (i) transforming a somatic embryogenic culture of a hybrid of P. rigida and P. taeda with a promoter operably linked to a desired polynucleotide, (ii) selecting transgenic cells from the transformed culture, (iii) culturing the transgenic cells to obtain at least one somatic embryo, (iv) germinating the embryo to obtain a transgenic plant, (v) growing the plant, and (vi) examining the plant for formation of strobili. In one embodiment, the promoter is a polynucleotide that is selected for testing promoter activity in a plant reproductive tissue. In another embodiment, the culture is transformed via Agrobacterium-mediated- or biolistic transformation. In a further embodiment, the desired polynucleotide is a reporter gene or an ablation construct. In this respect, in one embodiment, the ablation construct has the nucleic acid sequence depicted in any one of SEQ ID NOs. 13-15. In another embodiment, the construct may comprise the sequence depicted in any one of SEQ ID NOs. 18-26. In one embodiment, the plant of step (v) above is grown for 1 to 3 years.

Generally, a desired nucleic acid or desired polynucleotide of the present invention that is operably linked to a promoter or is incorporated into a plasmid or construct disclosed herein may comprise the sequence of any one of SEQ ID NOs. 5-8. In one embodiment, the desired nucleic acid or desired polynucleotide is a mutated barnase gene sequence. In a preferred embodiment, a reproductive-preferred promoter is operably linked to a polynucleotide that promote the genetic ablation of reproductive tissues in angiosperm and gymnosperm species. In a preferred embodiment, the polynucleotide is a mutant barnase gene. In one embodiment, the promoter comprises the sequence depicted in any one of SEQ ID NOs. 1-4 or 16. In another embodiment, the barnase gene has the sequence depicted in any one of SEQ ID NOs. 5-8 or encodes a polypeptide that comprises the sequence depicted in any one of SEQ ID NOs. 9-12. Any construct may comprise such a promoter-desired polynucleotide expression cassette.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1[A-C]—pWVR220 [PrMC2.400::barnaseH102E] (SEQ ID NO. 18)

FIG. 2[A-D]—pWVCZ20 [(AtAGenh)PrAG::GUS(intron)] (SEQ ID NO. 19)

FIG. 3[A-C]—pWVCZ23 [PrAG::barnaseE73G] (SEQ ID NO. 20)

FIG. 4[A-D]—pWVCZ24 [(AtAGenh)PrAG::barnaseE73G] (SEQ ID NO. 21)

FIG. 5[A-E]—pARB599B [PrMC2::barnaseH102E] (SEQ ID NO. 22). Short nucleotide sequences disclosed are residues 10431-10442, 10261-10271, 9885-9896, and 9569-9581 of SEQ ID NO: 22, respectively in order of appearance.

FIG. 6[A-G]—pARB639B [(AtAGenh)PrAG::barnaseE73G] (SEQ ID NO. 23). Short nucleotide sequences disclosed are residues 9906-9918, 13334-13346, 13650-13661, 14026-14036, and 14196-14207 of SEQ ID NO: 23, respectively in order of appearance.

FIG. 7[A-C]—pAGF243-[PrMC2.400-3::barnaseH102E](SEQ ID NO. 24)

FIG. 8[A-D]—pABDP010 [complementary copy of CZ28-bstar+UBQ10::NPTII::E9/LPAG1d4::bstar::NOST] (SEQ ID NO. 25)

FIG. 9[A-D]—pABDP04 [complementary copy of CZ28-bstar+UBQ10::NPTII::E9/LPAG1d4::bstar::NOST] (SEQ ID NO. 26)

FIG. 10—plasmid map for pWVR220

FIG. 11—plasmid map for pWVCZ20

FIG. 12—plasmid map for pWVCZ23

FIG. 13—plasmid map for pWVCZ24

FIG. 14—plasmid map for pARB599B

FIG. 15—plasmid map for pARB639B

FIG. 16—plasmid map for pAGF243

FIG. 17—plasmid map for pABDP010

FIG. 18—plasmid map for pABDP04

FIG. 19—pARB1005L [(AtAGenh)PrAG::barnaseE73G]

DETAILED DESCRIPTION OF THE EMBODIMENTS

The present invention relates to an isolated nucleic molecule comprising a polynucleotide having at least 95% sequence identity to a sequence selected from the group consisting of any of the polynucleotide sequences set forth below, i.e., SEQ ID NOs. 1-26 as well as those depicted in FIGS. 1-9 and portions thereof. The invention also provides functional fragments of the polynucleotide sequences disclosed herein. The invention further provides complementary nucleic acids, or fragments thereof, to any of the polynucleotide sequences disclosed herein, as well as a nucleic acid, comprising at least 15 contiguous bases, which hybridizes to any of the polynucleotide sequences disclosed herein.

The present invention also relates to an isolated polypeptide sequence comprising a polypeptide having a sequence selected from sequences set forth herein, such as those sequences depicted in SEQ ID NOs 9-12.

The present invention uses terms and phrases that are well known to those practicing the art. Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. Generally, the nomenclature used herein and the laboratory procedures in cell culture, molecular genetics, and nucleic acid chemistry and hybridization described herein are those well known and commonly employed in the art. Standard techniques are used for recombinant nucleic acid methods, polynucleotide synthesis, microbial culture, cell culture, tissue culture, transformation, transfection, transduction, analytical chemistry, organic synthetic chemistry, chemical syntheses, chemical analysis, and pharmaceutical formulation and delivery. Generally, enzymatic reactions and purification and/or isolation steps are performed according to the manufacturers' specifications. The techniques and procedures are generally performed according to conventional methodology. See, e.g., Sambrook & Russel, MOLECULAR CLONING: A LABORATORY MANUAL, 3^(rd) ed., Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., 2001.

Agrobacterium: as is well known in the field, Agrobacteria that are used for transforming plant cells are disarmed and virulent derivatives of, usually, Agrobacterium tumefaciens or Agrobacterium rhizogenes that contain a vector. The vector typically contains a desired polynucleotide that is located between the borders of a T-DNA.

Angiosperm: vascular plants having seeds enclosed in an ovary. Angiosperms are seed plants that produce flowers that bear fruits. Angiosperms are divided into dicotyledonous and monocotyledonous plants.

Angiosperm Reproductive Structure: includes the male and female tissues that comprise a flower. Typically, angiosperm flowers have four different floral organs: sepals (calyx), petals (corolla), stamens (androcecium), and pistils (gynoecium).

Angiosperm reproductive structure also embraces pre-male and pre-female reproductive structures. Pre-male and pre-female reproductive structures embrace cells and tissues that form before development and differentiation of male and female tissues.

Desired Polynucleotide: a desired polynucleotide of the present invention is a genetic element, such as a promoter, enhancer, or terminator, or gene or polynucleotide that is to be transcribed and/or translated in a transformed cell that comprises the desired polynucleotide in its genome. If the desired polynucleotide comprises a sequence encoding a protein product, the coding region may be operably linked to regulatory elements, such as to a promoter and a terminator, that bring about expression of an associated messenger RNA transcript and/or a protein product encoded by the desired polynucleotide. Thus, a “desired polynucleotide” may comprise a gene that is operably linked in the 5′- to 3′-orientation, a promoter, a gene that encodes a protein, and a terminator. Alternatively, the desired polynucleotide may comprise a gene or fragment thereof in an “antisense” orientation, the transcription of which produces nucleic acids that may form secondary structures that affect expression of an endogenous gene in the plant cell. A desired polynucleotide may also yield a double-stranded RNA product upon transcription that initiates RNA interference of a gene to which the desired polynucleotide is associated. A desired polynucleotide of the present invention may be positioned within a T-DNA, such that the left and right T-DNA border sequences flank or are on either side of the desired polynucleotide. The present invention envisions the stable integration of one or more desired polynucleotides into the genome of at least one plant cell. A desired polynucleotide may be mutated or may be a variant of its wild-type sequence. It is understood that all or part of the desired polynucleotide can be integrated into the genome of a plant. It also is understood that the term “desired polynucleotide” encompasses one or more of such polynucleotides. Thus, a T-DNA of the present invention may comprise one, two, three, four, five, six, seven, eight, nine, ten, or more desired polynucleotides.

Dicotyledonous plant (dicot): a flowering plant whose embryos have two seed halves or cotyledons, branching leaf veins, and flower parts in multiples of four or five. Examples of dicots include but are not limited to, Eucalyptus, Populus, Liquidambar, Acacia, teak, mahogany, cotton, tobacco, Arabidopsis, tomato, potato sugar beet, broccoli, cassaya, sweet potato, pepper, poinsettia, bean, alfalfa, soybean, carrot, strawberry, lettuce, oak, maple, walnut, rose, mint, squash, daisy, geranium, avocado, cactus, and Dichondra.

Endogenous: refers to a gene that is native to a plant genome.

Female reproductive tissues: include, for example, stigma, style, ovary, megaspore, female cones (ovuliferous cones), female gamete, female zygote, megasporocyte, and pre-female reproductive structures.

Female-Sterility Gene: refers to a nucleic acid molecule encoding an RNA, protein, or polypeptide that disrupts growth and development of a female gametophyte, female gamete, female zygote, seed, ovuliferous cone, or pre-female reproductive structure. A plant expressing a female-sterility gene produces no viable seed. There are many different mutations that can lead to female-sterility, involving all stages of development of a specific tissue of the female reproductive organ or pre-female reproductive structure.

Examples of female-sterility genes include, but in no way limiting, encode enzymes which catalyze the synthesis of phytohormones, such as: isopentenyl transferase which is an enzyme that catalyzes the first step in cytokinin biosynthesis and is encoded by gene 4 of Agrobacterium T-DNA; or one or both of the enzymes involved in the synthesis of auxin and encoded by gene 1 and gene 2 of Agrobacterium T-DNA. Yet other examples of female-sterility genes encode: glucanases; lipases such as phospholipase A.sub.2 (Verheij et al. Rev. Blochem. Pharmacol. 91:92-203 (1981)); lipid peroxidases; or plant cell wall inhibitors. Still other examples of female-sterility genes encode proteins toxic to plants cells, such as a bacterial toxin (e.g., the A-fragment of diphtheria toxin or botulin).

Still another example of a female-sterility gene is an antisense nucleic acid, or RNA involved in RNA interference (RNAi) such as small interfering RNA (siRNA), which can be useful for inhibiting or completely blocking the expression of a targeted gene. For example, an antisense or RNAi molecule of the invention encodes a nucleic acid strand complementary to a strand that is naturally transcribed in a plant's reproductive cells under the control of an endogenous promoter as described, for example, in European Patent Publication 0,223,399. Such an antisense nucleic acid or RNAi molecule may be capable of binding to the coding and/or non-coding portion of an RNA, naturally produced in the reproductive cell, so as to inhibit the translation of the naturally produced RNA. In one embodiment, an antisense nucleic acid and RNAi molecule of the invention can be expressed in flower, ovuliferous cone, seed, embryo, female gamete, female gametophyte, megasporocyte, and pre-female reproductive structures of the plant under the control of the endogenous promoter of the complementary endogenous DNA strand (or gene) of the plant.

Examples of such an antisense nucleic acid are the antisense DNA sequences of: the STMG-type genes, such as STMG07, STMG08, STMG4B12, and STMG3C9 genes. Jofuku and Goldberg. The Plant Cell 1: 1079-1093 (1989). The use of RNAi inhibition of gene expression is described generally in Paddison et al., Genes & Dev. 16: 948-958 (2002), and the use of RNAi to inhibit gene expression in plants is specifically described in WO 99/61631, both of which are herein incorporated by reference.

A further example of a female-sterility gene encodes a specific RNA enzyme (i.e., a “ribozyme”), capable of highly specific cleavage against a given target sequence as described by Haseloff and Gerlach et al. Nature 334, 585-591 (1998).

Fiber composition: as used herein, fiber composition refers to a trait that can be modified to change the structure, appearance, or use of fiber. Traits that determine fiber composition include but are not limited to fiber length, coarseness, strength, color, cross-sectional, width, and fiber density. For example, it is known that fiber length imparts strength, whereas fiber coarseness determines texture and flexibility.

In angiosperms, Floral Meristems initiate a floral structure having four different types of floral organs: sepals (calyx), petals (corolla), stamens (androecium), and pistils (gynoecium). Each floral organ is initated as a whorl, comprising concentric rings around the flanks of a floral meristem. The floral structure is supported by a pedicel or peduncle.

Flowering plants produce meiospores that are either microspores (male) or megaspores (female).

Foreign: “foreign,” with respect to a nucleic acid, means that that nucleic acid is derived from non-plant organisms, or derived from a plant that is not the same species as the plant to be transformed or is not derived from a plant that is not interfertile with the plant to be transformed, or does not belong to the species of the target plant. According to the present invention, foreign DNA or RNA may include nucleic acids that are naturally occurring in the genetic makeup of fungi, bacteria, viruses, mammals, fish or birds, but are not naturally occurring in the plant that is to be transformed. Thus, a foreign nucleic acid is one that encodes, for instance, a polypeptide that is not naturally produced by the transformed plant. A foreign nucleic acid does not have to encode a protein product.

Gene: A gene is a segment of a DNA molecule that contains all the information required for synthesis of a product, polypeptide chain or RNA molecule, and includes both coding and non-coding sequences.

Genetic element: a “genetic element” is any discreet nucleotide sequence including, but not limited to, a promoter, a gene, a terminator, an intron, an enhancer, a spacer, a 5′-untranslated region, a 3′-untranslated region, or a recombinase recognition site.

Genetic modification: stable introduction of DNA into the genome of certain organisms by applying methods in molecular and cell biology.

Gymnosperm: as used herein, refers to a seed plant that bears seed without ovaries. Examples of gymnosperms include conifers, cycads, ginkgos, and ephedras. In gymnosperms, reproductive shoot primordia develop into either male cones (staminate cones) or female cones (ovulate cones).

Gymnosperm Reproductive Structure: includes the male tissues that comprise male pollen cones (staminate cones) and female tissues that comprise female cones (ovulate cones). Gymnosperm reproductive structure also embraces pre-male and pre-female reproductive structures. Pre-male and pre-female reproductive structures embrace cells and tissues that form before development and differentiation of male and female tissues.

Introduction: as used herein, refers to the insertion of a nucleic acid sequence into a cell, by methods including infection, transfection, transformation or transduction.

Lignin: as used herein, refers to a polymeric composition composed of phenylpropanoid units, including polymerized derivatives of monolignols coniferyl, coumaryl, and sinapyl alcohol. Lignin quality refers to the ability of a lignin composition to impart strength to cell wall matrices, assist in the transport of water, and/or impede degradation of cell wall polysaccharides. Lignin composition or lignin structure may be changed by altering the relative amounts of each of monolignols or by altering the type of lignin. For example, guaiacyl lignins (derived from ferulic acid) are prominent in softwood species, whereas guaiacyl-syringyl lignins (derived from ferulic acid and sinapic acid) are characteristic of hardwood species. The degradation of lignin from softwoods, such as pine, requires substantially more alkali and longer incubations, compared with the removal of lignin from hardwoods. Lignin composition may be regulated by either up-regulation or down-regulation of enzymes involved lignin biosynthesis. For example, key lignin biosynthsesis enzymes include, but are not limited to, 4-coumaric acid: coenzyme A ligase (4CL), Cinnamyl Alcohol dehydrogenase (CAD), and Sinapyl Alcohol Dehydrogenase (SAD).

In angiosperms, male gametophytes or pollen grains develop in anthers, and the anthers are borne on stamens. Anther development occurs in two stages that correlate with pollen development. During phase I, sporogenic cells in the anther undergo microsporogenesis; nonsporogenic cells form the epidermis and tapetum. The tapetum is a tissue that surrounds sporogenic cells and provides nutritional materials for developing pollen. Additionally, the tapetum secretes the enzyme callase. During phase II, the anther enlarges and the filament elongates. At this time, pollen grains form, dehiscence occurs, and pollen grains are released.

In gymnosperms, such as conifers, a male pollen cone consists of an axis bearing a series of scales and two pollen sacs on the undersurface of each scale. Male cones consist of numerous microsporophylls that are tightly clustered in a spiral arrangement on a fertile shoot axis. Each microsporophyll bears two microsporangia, also called pollen sacs, on its lower, abaxial side. Within each microsporangium, sporangenous tissue lies. The sporangenous tissue consists of numerous diploid cells, called microsporocytes, which undergo meiosis. Around the periphery of each microsporangium lies the tapetum. Within the microsporangia, the microspores undergo mitosis and following two mitotic divisions, a four-celled male gametophyte is produced. The pollen grain comprises the microspore wall and the contained male gametophyte.

In gymnosperms, a female cone is formed by the fusion of numerous highly modified fertile shoots. In pines, for example, the female cone is comprised of individual units attached to a single, central axis. The individual units are made of an ovuliferous scale (ovule-bearing) and a subtending bract that is almost completely fused to the ovuliferous scale above it. Each ovuliferous scale is formed by the fusion of megasporophylls and other fertile shoot components. On the upper, adaxial surface of each ovuliferous scale are two ovules. The ovules are oriented with their micropyles toward the central cone axis and are partially imbedded in the tissues of the ovuliferous scale. Each ovule has an integument (one multicellular layer) that, except for the micropyles, completely surrounds the megasporangium. The integument or nucellus functions as the nutritive tissue and each nucellus has a single megasporocyte. The megasporocyte is the diploid cell that undergoes meiosis. The micropylar chamber is located within each ovule between the nucellus and the micropyle.

Male reproductive tissues: include, for example, pollen grains, tapetum, anther, filament, pollen mother cells, microspores, microsporocyte, male pollen cones (staminate cones), pollen sacs, and pre-male reproductive structures.

Male-Sterility Gene: refers to a nucleic acid molecule encoding an RNA, protein, or polypeptide that disturbs the proper metabolism, functioning and/or development of any reproductive cell in which the male-sterility gene is expressed, thereby leading to the death and/or destruction of any such reproductive cell. There are many different mutations that can lead to male-sterility, involving all stages of development of a specific tissue of the male reproductive organ or pre-male reproductive structure.

The expression of a male-sterility gene, for example, renders a plant incapable of producing fertile pollen. The expression of a male-sterility gene in a transformed plant may result in a plant producing pollen, though the pollen may be aberrant and non-functional for fertilization. For example, a non-functional pollen may fail to germinate a pollen tube. While by no means limiting, examples of male-sterility genes encode: RNases such as RNase T1 (which degrades RNA molecules by hydrolyzing the bond after any guanine residue) and Barnase; DNases such as an endonuclease (e.g., EcoRI); or proteases such as a papain (e.g., papain zymogen and papain active protein).

Other male-sterility genes encode enzymes which catalyze the synthesis of phytohormones. For example, isopentenyl transferase, an enzyme that catalyzes the first step in cytokinin biosynthesis, and enzymes involved in the synthesis of auxin may be used for inducing male-sterility. Other male-sterility genes encode glucanases; lipases such as phospholipase A.sub.2 (Verheij et al. Rev. Biochem. Pharmacol. 91: 92-203 (1981)); lipid peroxidases; or plant cell wall inhibitors. Still other examples of male-sterility genes encode proteins toxic to a plants cell, such as a bacterial toxin (e.g., the B-fragment of diphtheria toxin or botulin).

Still another example of a male-sterility gene is an antisense nucleic acid, or RNA involved in RNA interference (RNAi) such as small interfering RNA (siRNA), which can be useful for inhibiting or completely blocking the expression of a targeted gene. For example, an antisense or RNAi molecule of the invention encodes a nucleic acid strand complementary to a strand that is naturally transcribed in a plant's reproductive cells under the control of an endogenous promoter as described, for example, in European Patent Publication 0,223,399. Such an antisense nucleic acid or RNAi molecule may be capable of binding to the coding and/or non-coding portion of an RNA, naturally produced in the reproductive cell, so as to inhibit the translation of the naturally produced RNA. In one embodiment, an antisense nucleic acid and RNAi molecule of the invention can be expressed in pollen grains, tapetum, anther, filament, pollen mother cells, microspores, microsporocyte, male pollen cones (staminate cones), pollen sacs, and pre-male reproductive structures.

Microsporogenesis is the process by which a diploid cell, the microsporocyte, undergoes meiotic division to produce four, haploid microspores (microspore tetrad). The microspore tetrad is encased in a callose cell wall.

In angiosperms, microsporogenesis occurs in the stamens, the male reproductive tissues of a flower. Each stamen has a filament and an anther. Each anther has one to four chambers, called pollen sacs or anther sacs. Each anther sac produces numerous microsporocytes, also called pollen mother cells.

In gymnosperms, microsporogenesis occurs in the microsporangia or pollen sacs of the microsporophyll. Within the microsporangia, the microspores undergo mitosis and produce a four-celled male gametophyte. A gymnosperm pollen grain comprises the microspore wall and the contained male gametophyte.

Monocotyledonous plant (monocot): a flowering plant having embryos with one cotyledon or seed leaf, parallel leaf veins, and flower parts in multiples of three. Examples of monocots include, but are not limited to, turfgrass, maize, rice, oat, wheat, barley, sorghum, orchid, iris, lily, onion, and palm. Examples of turfgrass include, but are not limited to, Agrostis spp. (bentgrass species including colonial bentgrass and creeping bentgrasses), Poa pratensis (kentucky bluegrass), Lolium spp. (ryegrass species including annual ryegrass and perennial ryegrass), Festuca arundinacea (tall fescue) Festuca rubra commutata (fine fescue), Cynodon dactylon (common bermudagrass varieties including Tifgreen, Tifway II, and Santa Ana, as well as hybrids thereof); Pennisetum clandestinum (kikuyugrass), Stenotaphrum secundatum (st. augustinegrass), Zoysia japonica (zoysiagrass), and Dichondra micrantha.

Operably linked: combining two or more molecules in such a fashion that in combination they function properly in a plant cell. For instance, a promoter is operably linked to a structural gene when the promoter controls transcription of the structural gene.

Phenotype: phenotype is a distinguishing feature or characteristic of a plant, which may be altered according to the present invention by integrating one or more “desired polynucleotides” and/or screenable/selectable markers into the genome of at least one plant cell of a transformed plant. The “desired polynucleotide(s)” and/or markers may confer a change in the phenotype of a tranformed plant by modifying any one of a number of genetic, molecular, biochemical, physiological, morphological, or agronomic characteristics or properties of the transformed plant cell or plant as a whole. Thus, expression of one or more, stably integrated desired polynucleotide(s) in a plant genome may yield a phenotype selected from the group consisting of, for example, increased drought tolerance, enhanced cold and frost tolerance, improved vigor, enhanced color, enhanced health and nutritional characteristics, improved storage, enhanced yield, enhanced salt tolerance, enhanced heavy metal tolerance, increased disease tolerance, increased insect tolerance, increased water-stress tolerance, enhanced sweetness, improved vigor, improved taste, improved texture, decreased phosphate content, increased germination, increased micronutrient uptake, improved starch composition, and improved flower longevity.

Plant tissue: a “plant” is any of various photosynthetic, eukaryotic, multicellular organisms of the kingdom Plantae characteristically producing embryos, containing chloroplasts, and having cellulose cell walls. A part of a plant, i.e., a “plant tissue” may be transformed according to the methods of the present invention to produce a transgenic plant. Many suitable plant tissues can be transformed according to the present invention and include, but are not limited to, somatic embryos, pollen, leaves, stems, calli, stolons, microtubers, and shoots. Thus, the present invention envisions the transformation of angiosperm and gymnosperm plants such as turfgrass, wheat, maize, rice, barley, oat, sugar beet, potato, tomato, tobacco, alfalfa, lettuce, carrot, strawberry, cassaya, sweet potato, geranium, soybean, oak, apple, grape, pine, fir, acacia, eucalyptus, walnut, and palm. According to the present invention “plant tissue” also encompasses plant cells. Plant cells include suspension cultures, callus, embryos, meristematic regions, callus tissue, leaves, roots, shoots, gametophytes, sporophytes, pollen, seeds and microspores. Plant tissues may be at various stages of maturity and may be grown in liquid or solid culture, or in soil or suitable media in pots, greenhouses or fields. A plant tissue also refers to any clone of such a plant, seed, progeny, propagule whether generated sexually or asexually, and descendents of any of these, such as cuttings or seed. Of particular interest are conifers such as pine, fir, and spruce, monocots such as Kentucky bluegrass, creeping bentgrass, maize, and wheat, and dicots such as cotton, tomato, lettuce, Arabidopsis, tobacco, apple and geranium.

Plant transformation and cell culture: broadly refers to the process by which plant cells are genetically modified and transferred to an appropriate plant culture medium for maintenance, further growth, and/or further development. Such methods are well known to the skilled artisan.

Pollen refers to the microspores of seeds plants and the powdery mass of microspores shed from anthers and staminate pollen cones.

Pre-female reproductive structures: refers to cells and tissues that form before development and differentiation of female tissues in angiosperm and gymnosperm species.

Pre-male reproductive structures: refers to cells and tissues that form before development and differentiation of male tissues in angiosperm and gymnosperm species.

Progeny: a “progeny” of the present invention, such as the progeny of a transgenic plant, is one that is born of, begotten by, or derived from a plant or the transgenic plant. Thus, a “progeny” plant, i.e., an “F1” generation plant is an offspring or a descendant of the transgenic plant produced by the inventive methods. A progeny of a transgenic plant may contain in at least one, some, or all of its cell genomes, the desired polynucleotide that was integrated into a cell of the parent transgenic plant by the methods described herein. Thus, the desired polynucleotide is “transmitted” or “inherited” by the progeny plant. The desired polynucleotide that is so inherited in the progeny plant may reside within a T-DNA construct, which also is inherited by the progeny plant from its parent. The term “progeny” as used herein also may be considered to be the offspring or descendants of a group of plants.

Promoter: is intended to mean a nucleic acid, preferably DNA, that binds RNA polymerase and/or other transcription regulatory elements. As with any promoter, the promoter sequences of the current present invention will facilitate or control the transcription of DNA or RNA to generate an mRNA molecule from a nucleic acid molecule that is operably linked to the promoter. As stated earlier, the RNA generated may code for a protein or polypeptide or may code for an RNA interfering, or antisense molecule.

A promoter, as used herein, may also include regulatory elements. Conversely, a regulatory element may also be separate from a promoter. Regulatory elements confer a number of important characteristics upon a promoter region. Some elements bind transcription factors that enhance the rate of transcription of the operably linked nucleic acid. Other elements bind repressors that inhibit transcription activity. The effect of transcription factors on promoter activity may determine whether the promoter activity is high or low, i.e. whether the promoter is “strong” or “weak.”

A plant promoter is a promoter capable of initiating transcription in plant cells, whether or not its origin is a plant cell. Exemplary plant promoters include, but are not limited to, those that are obtained from plants, plant viruses, and bacteria such as Agrobacterium or Rhizobium which comprise genes expressed in plant cells. Examples of promoters under developmental control include promoters that preferentially initiate transcription in certain tissues, such as tapetum, xylem, leaves, roots, or seeds. Such promoters are referred to as tissue preferred promoters. Promoters which initiate transcription only in certain tissues are referred to as tissue specific promoters. A cell type specific promoter primarily drives expression in certain cell types in one or more organs, for example, vascular cells in roots or leaves. An inducible or repressible promoter is a promoter which is under environmental control. Examples of environmental conditions that may effect transcription by inducible promoters include anaerobic conditions, heat, or the presence of light. Tissue specific, tissue preferred, cell type specific, and inducible promoters constitute the class of non-constitutive promoters. A constitutive promoter is a promoter which is active under most environmental conditions, and in most plant parts.

Polynucleotide is a nucleotide sequence comprising a gene coding sequence or a fragment thereof (comprising at least 15 consecutive nucleotides, at least 30 consecutive nucleotides, or at least 50 consecutive nucleotides), a promoter, an intron, an enhancer region, a polyadenylation site, a translation initiation site, 5′ or 3′ untranslated regions, a reporter gene, a selectable marker or the like. The polynucleotide may comprise single stranded or double stranded DNA or RNA. The polynucleotide may comprise modified bases or a modified backbone. The polynucleotide may be genomic, an RNA transcript (such as an mRNA) or a processed nucleotide sequence (such as a cDNA). The polynucleotide may comprise a sequence in either sense or antisense orientations.

An isolated polynucleotide is a polynucleotide sequence that is not in its native state, e.g., the polynucleotide is comprised of a nucleotide sequence not found in nature, or the polynucleotide is separated from nucleotide sequences to which it typically is in proximity, or is in proximity to nucleotide sequences with which it typically is not in proximity.

Regenerability: as used herein, refers to the ability of a plant to redifferentiate from a de-differentiated tissue.

Reproductive-preferred promoter refers to a promoter preferentially expressed in a plant's reproductive tissue. Reproductive plant tissue includes both male and female portions of the reproductive structure, as well as pre-male and pre-female reproductive structures. Male reproductive tissues include, for example, pollen grains, tapetum, anther, filament, pollen mother cells, microspores, male pollen cones (staminate cones), and pre-male reproductive structures. Female reproductive tissues include, for example, stigma, style, ovary, megaspores, ovuliferous scale, bract, female pollen cones (ovuliferous cones), and pre-female reproductive structures. Accordingly, a reproductive-preferred promoter may be preferentially expressed in any angiosperm reproductive structure or gymnosperm reproductive structure.

Seed: a “seed” may be regarded as a ripened plant ovule containing an embryo, and a propagative part of a plant, as a tuber or spore. Seed may be incubated prior to Agrobacterium-mediated transformation, in the dark, for instance, to facilitate germination. Seed also may be sterilized prior to incubation, such as by brief treatment with bleach. The resultant seedling can then be exposed to a desired strain of Agrobacterium.

Selectable/screenable marker: a gene that, if expressed in plants or plant tissues, makes it possible to distinguish them from other plants or plant tissues that do not express that gene. Screening procedures may require assays for expression of proteins encoded by the screenable marker gene. Examples of such markers include the beta glucuronidase (GUS) gene and the luciferase (LUX) gene. Examples of selectable markers include the neomycin phosphotransferase (NPTII) gene encoding kanamycin and geneticin resistance, the hygromycin phosphotransferase (HPT or APHIV) gene encoding resistance to hygromycin, acetolactate synthase (als) genes encoding resistance to sulfonylurea-type herbicides, genes (BAR and/or PAT) coding for resistance to herbicides which act to inhibit the action of glutamine synthase such as phosphinothricin (Liberty or Basta), or other similar genes known in the art.

Sequence identity: as used herein, “sequence identity” or “identity” in the context of two nucleic acid or polypeptide sequences includes reference to the residues in the two sequences which are the same when aligned for maximum correspondence over a specified region.

As used herein, percentage of sequence identity means the value determined by comparing two optimally aligned sequences over a comparison window, wherein the portion of the polynucleotide sequence in the comparison window may comprise additions or deletions (i.e., gaps) as compared to the reference sequence (which does not comprise additions or deletions) for optimal alignment of the two sequences. The percentage is calculated by determining the number of positions at which the identical nucleic acid base occurs in both sequences to yield the number of matched positions, dividing the number of matched positions by the total number of positions in the window of comparison and multiplying the result by 100 to yield the percentage of sequence identity.

Stamen: refers to the organ of the flower that produces the male gamete and includes an anther and filament.

Tapetum: refers to a layer of cells surrounding microsporogenous cells in the anther of an angiosperm or the microsporangeous cells within a staminate cone of a gymnosperm. Given its close proximity to the developing microspores, the tapetum likely provides nutrients, such as reducing sugars, amino acids and lipids to the developing microspores. Reznickova, C. R., Acad. Bulg. Sci. 31:1067 (1978). Nave, et al., J. Plant Physiol. 125:451 (1986). Sawhney, et al., J. Plant Physiol 125:467 (1986). Tapetal cells also produce beta(1,3) glucanase (callase) which promotes microspore release by digesting the callose cell wall. Therefore, a fragile relationship exists between the tapetum and the microsporogenous cells, and any disruption of tapetal function is likely to result in non-functional pollen grains. It has been shown, for example, lesions in tapetal biogenesis result in male sterility mutants (Kaul, “Male Sterility in Higher Plants” in Monographs on Theoretical and Applied Genetics; Frankel et al. eds.; Springer Verlag; Vol. 10; pp. 15-95; (1988)). Therefore, a gene encoding callase can be used for disrupting male reproductive development. Thus, a failure of the microspores to develop into mature pollen grains can be induced using, for example, a recombinant DNA molecule that comprises a gene capable of disrupting tapetal function under the control of tapetum-specific regulatory sequences.

Transcription factor: Transcription factor refers to a polypeptide sequence that regulates the expression of a gene or genes by either directly binding to one or more nucleotide sequences associated with a gene coding sequence or indirectly affecting the activity of another polypeptide(s) that bind directly to one or more nucleotide sequences associated with a gene coding sequence. A transcription factor may activate (up-regulate) or repress (down-regulate) expression of a gene or genes. A transcription factor may contain a DNA binding domain, an activation domain, or a domain for protein-protein interactions. In the present invention, a transcription factor is capable of at least one of (1)binding to a nucleic acid sequence or (2) regulating expression of a gene in a plant.

Transcription and translation terminators: The expression DNA constructs of the present invention typically have a transcriptional termination region at the opposite end from the transcription initiation regulatory element. The transcriptional termination region may be selected, for stability of the mRNA to enhance expression and/or for the addition of polyadenylation tails added to the gene transcription product.

Transfer DNA (T-DNA): an Agrobacterium T-DNA is a genetic element that is well-known as an element capable of integrating a nucleotide sequence contained within its borders into another genome. In this respect, a T-DNA is flanked, typically, by two “border” sequences. A desired polynucleotide of the present invention and a selectable marker may be positioned between the left border-like sequence and the right border-like sequence of a T-DNA. The desired polynucleotide and selectable marker contained within the T-DNA may be operably linked to a variety of different, plant-specific (i.e., native), or foreign nucleic acids, like promoter and terminator regulatory elements that facilitate its expression, i.e., transcription and/or translation of the DNA sequence encoded by the desired polynucleotide or selectable marker.

Transformation of plant cells: A process by which a nucleic acid is stably inserted into the genome of a plant cell. Transformation may occur under natural or artificial conditions using various methods well known in the art. Transformation may rely on any known method for the insertion of nucleic acid sequences into a prokaryotic or eukaryotic host cell, including Agrobacterium-mediated transformation protocols, viral infection, whiskers, electroporation, microinjection, polyethylene glycol-treatment, heat shock, lipofection and particle bombardment.

Transgenic plant: a transgenic plant of the present invention is one that comprises at least one cell genome in which an exogenous nucleic acid has been stably integrated. According to the present invention, a transgenic plant is a plant that may comprise only one genetically modified cell and cell genome, or it may comprise several or many genetically modified cells, or all of the cells may be genetically modified. A transgenic plant of the present invention may be one in which expression of the desired polynucleotide, i.e., the exogenous nucleic acid, occurs in only certain parts of the plant. Thus, a transgenic plant may contain only genetically modified cells in certain parts of its structure.

Variant: a “variant,” as used herein, is understood to mean a nucleotide sequence that deviates from the reference (i.e., native, standard, or given) nucleotide sequence of a particular gene. The terms, “isoform,” “isotype,” and “analog” also refer to “variant” forms of a nucleotide sequence.

Variant may also refer to a “shuffled gene” such as those described in Maxygen-assigned patents. For instance, a variant of the present invention may include variants of sequences and desired polynucleotides that are modified according to the methods and rationale disclosed in U.S. Pat. No. 6,132,970, which is incorporated herein by reference.

Vegetative growth: this well-accepted term of art refers to the general, overall development of a plant. To elaborate, after reproduction, meristem cells differentiate into apical-, lateral meristems that ultimately develop into roots and shoots and, later, into leaves and flowers, for instance. Shoot and root architecture, branching patterns, development of stems, axillary buds, and primordial cells into leaves, petals, flowers, and fruit etc. are all considered “vegetative” and part of the “vegetative growth” cycle of a plant. The rate of development of such features depends on a variety of factors, such as the species of the plant, photosynthesis, availability of nutrients, and the general environment in which the plant is growing.

Genetics also plays an important literal and figurative role in shaping a plant's development. For instance, the “simple” or “compound” shape of a leaf, i.e., whether it is characterized by smooth-edges, deep lobes, individual leaflets, or tendrils can be dictated by gene expression. The “LEAFY” gene, for example, plays a role in compound leaf development and is essential for the transition from vegetative to reproductive development. LEAFY was identified in Arabidopsis and snapdragon, and has homologues in other angiosperms. The pea homologue, Unifoliata, has a mutant phenotype in which compound leaves are reduced to simple leaves, which may indicate a regulatory relationship between shoots and compound leaves.

Similarly, the acacia mutant, “tl,” converts tendrils to leaflets, whilst the mutation, afilia, “af,” converts leaflet to tendrils. The “af tl” double mutant has a complex architecture, resembling a parsley leaf. Likewise, other genes, which are expressed throughout such “vegetative” plant cells and tissues, coordinate and connote developmental, physiological, and structural characteristics to other discreet parts of the plant. Thus, there are many “vegetative-specific” genes that are expressed, either specifically or predominantly, in all vegetative tissues, such as roots, shoots, stems, and leaves, or which are vegetative-tissue specific. The promoters of such genes are, therefore, useful in directing the expression of a desired gene, endogenous or foreign, to a particular vegetative tissue. Thus, it is possible to preferentially express a gene product in one or more vegetative tissues, whilst avoiding expression of that same product in non-vegetative tissues, such as in reproductive tissue cells.

Wood composition: refers to a trait that can be modified to change the structure, appearance, or use of wood. While not limiting, traits that determine wood composition include cell wall thickness, cell length, cell size, lumen size, cell density, microfibril angle, tensile strength, tear strength, wood color, and length and frequency of cell division.

Wood pulp: refers to fiber generated from wood having varying degrees of purification. Wood pulp can be used for producing paper, paper board, and chemical products.

It is understood that the present invention is not limited to the particular methodology, protocols, vectors, and reagents, etc., described herein, as these may vary. It is also to be understood that the terminology used herein is used for the purpose of describing particular embodiments only, and is not intended to limit the scope of the present invention. It must be noted that as used herein and in the appended claims, the singular forms “a,” “an,” and “the” include plural reference unless the context clearly dictates otherwise. Thus, for example, a reference to “a gene” is a reference to one or more genes and includes equivalents thereof known to those skilled in the art and so forth. Indeed, one skilled in the art can use the methods described herein to express any native gene (known presently or subsequently) in plant host systems.

Nucleic Acids

By “isolated” nucleic acid molecule(s) is intended a nucleic acid molecule, DNA or RNA, which has been removed from its native environment. For example, recombinant DNA molecules contained in a vector are considered isolated for the purposes of the present invention. Further examples of isolated DNA molecules include recombinant DNA molecules maintained in heterologous host cells or purified (partially or substantially) DNA molecules in solution. Isolated RNA molecules include in vitro RNA transcripts of the DNA molecules of the present invention. Isolated nucleic acid molecules, according to the present invention, further include such molecules produced synthetically.

Nucleic acid molecules of the present invention may be in the form of RNA, such as mRNA, or in the form of DNA, including, for instance, cDNA and genomic DNA obtained by cloning or produced synthetically. The DNA or RNA may be double-stranded or single-stranded. Single-stranded DNA may be the coding strand, also known as the sense strand, or it may be the non-coding strand, also referred to as the anti-sense strand.

Unless otherwise indicated, all nucleotide sequences determined by sequencing a DNA molecule herein were determined using an automated DNA sequencer (such as the Model 3700 from Applied Biosystems, Inc.), and all amino acid sequences of polypeptides encoded by DNA molecules determined herein were predicted by translation of a DNA sequence determined as above. Therefore, as is known in the art for any DNA sequence determined by this automated approach, any nucleotide sequence determined herein may contain some errors. Nucleotide sequences determined by automation are typically at least about 95% identical, more typically at least about 96% to at least about 99.9% identical to the actual nucleotide sequence of the sequenced DNA molecule. The actual sequence can be more precisely determined by other approaches including manual DNA sequencing methods well known in the art. As is also known in the art, a single insertion or deletion in a determined nucleotide sequence compared to the actual sequence will cause a frame shift in translation of the nucleotide sequence such that the predicted amino acid sequence encoded by a determined nucleotide sequence may be completely different from the amino acid sequence actually encoded by the sequenced DNA molecule, beginning at the point of such an insertion or deletion.

Unless otherwise indicated, each “nucleotide sequence” set forth herein is presented as a sequence of deoxyribonucleotides (abbreviated A, G, C and T). However, by “nucleotide sequence” of a nucleic acid molecule or polynucleotide is intended, for a DNA molecule or polynucleotide, a sequence of deoxyribonucleotides, and for an RNA molecule or polynucleotide, the corresponding sequence of ribonucleotides (A, G, C and U) where each thymidine deoxynucleotide (T) in the specified deoxynucleotide sequence in is replaced by the ribonucleotide uridine (U). For instance, reference to an RNA molecule having the sequence of SEQ ID NO: 1 set forth using deoxyribonucleotide abbreviations is intended to indicate an RNA molecule having a sequence in which each deoxynucleotide A, G or C of SEQ ID NO: 1 has been replaced by the corresponding ribonucleotide A, G or C, and each deoxynucleotide T has been replaced by a ribonucleotide U.

The present invention is also directed to fragments of the isolated nucleic acid molecules described herein. By a fragment of an isolated DNA molecule having the nucleotide sequences disclosed herein is intended DNA fragments at least 15 nucleotides, at least 20 nucleotides, at least 30 nucleotides in length, which are useful as diagnostic probes and primers is discussed in more detail below. Of course larger nucleic acid fragments of up to the entire length of the nucleic acid molecules of the present invention are also useful diagnostically as probes, according to conventional hybridization techniques, or as primers for amplification of a target sequence by the polymerase chain reaction (PCR), as described, for instance, in Molecular Cloning, A Laboratory Manual, 3rd. edition, edited by Sambrook, J and Russel, D. W., (2001), Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., the entire disclosure of which is hereby incorporated herein by reference.

By a fragment at least 20 nucleotides in length, for example, is intended fragments which include 20 or more contiguous bases from the nucleotide sequence of the as disclosed herein, i.e., SEQ ID NOs. 1-26. Nucleic acids comprising the nucleotide sequences disclosed herein can be generated using conventional methods of DNA synthesis which will be routine to the skilled artisan. For example, restriction endonuclease cleavage or shearing by sonication could easily be used to generate fragments of various sizes. Alternatively, the DNA fragments of the present invention could be generated synthetically according to known techniques.

In another aspect, the invention provides an isolated nucleic acid molecule comprising a polynucleotide which hybridizes under stringent hybridization conditions to a portion of the polynucleotide in a nucleic acid molecule of the invention described above. By a polynucleotide which hybridizes to a “portion” of a polynucleotide is intended a polynucleotide (either DNA or RNA) hybridizing to at least about 15 nucleotides, at least about 20 nucleotides, at least about 30 nucleotides, and more than 30 nucleotides of the reference polynucleotide. These fragments that hybridize to the reference fragments are useful as diagnostic probes and primers. A probe, as used herein is defined as at least about 50 contiguous bases of one of the nucleic acids disclosed herein, i.e., SEQ ID NOs. 1-8 and 13-26. For the purpose of the invention, two sequences hybridize when they form a double-stranded complex in a hybridization solution of 6×SSC, 0.5% SDS, 5×Denhardt's solution and 100 μg of non-specific carrier DNA. See Ausubel et al, section 2.9, supplement 27 (1994). Sequences may hybridize at “moderate stringency,” which is defined as a temperature of 60° C. in a hybridization solution of 6×SSC, 0.5% SDS, 5×Denhardt's solution and 100 μg of non-specific carrier DNA. For “high stringency” hybridization, the temperature is increased to 68° C. Following the moderate stringency hybridization reaction, the nucleotides are washed in a solution of 2×SSC plus 0.05% SDS for five times at room temperature, with subsequent washes with 0.1×SSC plus 0.1% SDS at 60° C. for 1 h. For high stringency, the wash temperature is increased to 68° C. For the purpose of the invention, hybridized nucleotides are those that are detected using 1 ng of a radiolabeled probe having a specific radioactivity of 10,000 cpm/ng, where the hybridized nucleotides are clearly visible following exposure to X-ray film at −70° C. for no more than 72 hours.

As mentioned previously, the present application is directed to such nucleic acid molecules which are at least 90%, 95%, 96%, 97%, 98%, 99% or 100% identical to a nucleic acid sequence described above. One embodiment encompasses nucleic acid molecules which are at least 95%, 96%, 97%, 98%, 99% or 100% identical to the nucleic acid sequence shown in SEQ ID NOs. 1-8 and 13-26. By a polynucleotide having a nucleotide sequence at least, for example, 95% “identical” to a reference nucleotide sequence, is intended that the nucleotide sequence of the polynucleotide is identical to the reference sequence except that the polynucleotide sequence may include up to five point mutations per each 100 nucleotides of the reference nucleotide sequence. In other words, to obtain a polynucleotide having a nucleotide sequence at least 95% identical to a reference nucleotide sequence, up to 5% of the nucleotides in the reference sequence may be deleted or substituted with another nucleotide, or a number of nucleotides up to 5% of the total nucleotides in the reference sequence may be inserted into the reference sequence. These mutations of the reference sequence may occur at the 5′ or 3′ terminal positions of the reference nucleotide sequence or anywhere between those terminal positions, interspersed either individually among nucleotides in the reference sequence or in one or more contiguous groups within the reference sequence.

As a practical matter, whether any particular nucleic acid molecule is at least 95%, 96%, 97%, 98% or 99% identical to a reference nucleotide sequence refers to a comparison made between two molecules using standard algorithms well known in the art. Although any sequence algorithm can be used to define sequence identity, for clarity, the present invention defines identity with reference to the Basis Local Alignment Search Tool (BLAST) algorithm (Altschul et al., J. Mol. Biol. 215:403-410 (1990)), where a promoter sequence set forth in the disclosure is used as the reference sequence to define the percentage identity of polynucleotide homologs over its length. The choice of parameter values for matches, mismatches, and inserts or deletions is arbitrary, although some parameter values have been found to yield more biologically realistic results than others.

When using BLAST or any other sequence alignment program to determine whether a particular sequence is, for instance, 95% identical to a reference sequence according to the present invention, the parameters are set, of course, such that the percentage of identity is calculated over the full length of the reference nucleotide sequence and that gaps in homology of up to 5% of the total number of nucleotides in the reference sequence are allowed.

Relatedness between two polynucleotides also may be described by reference to their ability to hybridize to form double-stranded complexes by the formation of complementary base pairs. Hybridization conditions have been described previously herein. An increase in temperature can be used to break apart these complexes. The more structurally identical two sequences are, the higher the temperature required to break them apart or “melt” them. The temperature required to melt a double-stranded complex is called the “T_(m).” The relationship between the T_(m) and other hybridization parameters is given by:

T _(m)(° C.)=81.5+16.6(log₁₀[Na⁺])+0.41(fraction G+C)−0.63(% formamide)−(600/l),

where T_(m) is the melting temperature of a DNA duplex consisting of the probe and its target; and l=the length of the hybrid in base pairs, provided l>100 base pairs. Bolton et al., Proc. Natl. Acad. Sci. 48:1390 (1962). Generally, a change of 1° C. in the melting point represents from 0.7% to 3.2% difference in DNA sequence similarity. Bonner et al., Journal of Molecular Biology 81:123-35 (1973); McCarthy et al., In EVOLUTION OF GENETIC SYSTEMS, H. H. Smith (ed.), Brookhaven Symposium in Biology No. 23, Gordon and Breach, New York, pp. 1-43 (1972). The formation of a stable DNA duplex at 60° C. typically requires at least an 80% sequence identity between sequences. Sibley et al., ACTA 1: 83-121 (Proceedings of the 18th International Ornithological Congress, Moscow, Aug. 16-24, 1982, Academy of Sciences of the USSR).

In one embodiment, the nucleic acids of the present invention confer preferential expression of polypeptides or proteins in the reproductive tissues of angiosperm and gymnosperm plants. The nucleic acids of the present invention can also preferentially direct the expression of antisense RNA, or RNA involved in RNA interference (RNAi) such as small interfering RNA (siRNA), in the reproductive tissue of plants, which can be useful for inhibiting or completely blocking the expression of targeted genes.

Reproductive plant tissue includes both male and female portions of reproductive organs. Male tissues include, for example, pollen, tapetum, anther, filament, pollen mother cells, microspores, male pollen cones (staminate cones), and pre-male reproductive structures. Female reproductive tissues include, for example, stigma, style, ovary, megaspores, female cones (ovuliferous cones), and pre-female reproductive structures.

Reproductive-preferred promoter refers to a promoter preferentially expressed in a plant's reproductive tissue. Reproductive plant tissue includes both male and female portions of the reproductive structure, as well promoters expressed in pre-male and pre-female reproductive structures. Male reproductive tissues include, for example, pollen grains, tapetum, anther, filament, pollen mother cells, microspores, and pollen cones. Female reproductive tissues include, for example, stigma, style, ovary, megaspores, and ovuliferous cones. Accordingly, a reproductive-preferred promoter may be preferentially expressed in any reproductive structure of any angiosperm or gymnosperm species, in addition to expression in any pre-male or pre-female tissue of gymnosperm and angiosperm species.

In one embodiment, a reproductive-preferred promoter confers expression of a gene in a male-reproductive tissue. In one embodiment, a reproductive-preferred promoter confers gene expression in the anther, pollen or filament cells of an angiosperm species. In a further embodiment, the reproductive-preferred promoter confers gene expression in the tapetum or anther epidermal cells. In another embodiment, a reproductive-preferred promoter confers gene expression in a male pollen cone, tapetum, microsporophyll, or any other male reproductive tissue present in a gymnosperm. For both angiosperm and gymnosperm species, a reproductive-preferred promoter confers gene expression in a pre-male or pre-female reproductive structure.

A reproductive-preferred promoter can be used for example, to render a plant male-sterile. For example, a reproductive-preferred promoter can be operably linked to a cytotoxic gene, such that expression of the cytotoxic gene in a male reproductive tissue renders the plant incapable of producing fertile male gametes. In another embodiment, a reproductive-preferred promoter may be selected and isolated such that the promoter does not express an operably-linked gene in a non-reproductive tissue, such as a vegetative tissue.

In one embodiment, a reproductive-preferred promoter confers expression of a gene in a female-reproductive tissue. In one embodiment, a reproductive-preferred promoter confers gene expression in the stigma, style, or ovary of an angiosperm species. In another embodiment, a reproductive-preferred promoter confers gene expression in a female cone (ovuliferous cone), megasporophyll, or any other female reproductive tissue present in a gymnosperm species. For both angiosperm and gymnosperm species, a reproductive-preferred promoter confers gene expression in a pre-male or pre-female reproductive structure.

A reproductive-preferred promoter can be used for example, to render a plant female-sterile. In one embodiment, a reproductive-preferred promoter can be operably linked to a cytotoxic gene, such that expression of the cytotoxic gene in a female reproductive tissue renders the plant incapable of producing fertile female gametes, female zygote, and/or seed. In another embodiment, a reproductive-preferred promoter may be selected and isolated such that the promoter does not express an operably-linked gene in a non-reproductive tissue, such as a vegetative tissue.

For example, a reproductive-preferred promoter may be identified by searching for an mRNA which is only present during reproductive development. Additionally, a reproductive-preferred promoter may be present in pre-male and pre-female reproductive tissues. In one embodiment, a reproductive-preferred promoter is identified from mRNA present during development of a plant's male reproductive tissues, including, for example, anthers, pollen, filament, male staminate cones, and pre-male reproductive tissues. In one embodiment, a reproductive-preferred promoter is identified from mRNA present during development of a plant's female reproductive tissues, including, for example, stigma, style, ovary, ovuliferous cones, and pre-female reproductive tissues. Following identification and isolation of a reproductive-preferred mRNA, cDNA is prepared from this reproductive-preferred mRNA. The resultant cDNA may be used as a probe to identify the regions in a plant genome containing DNA coding for a reproductive-preferred mRNA. Once a DNA has been identified, the sequence upstream (i.e., 5′) from the DNA coding for a reproductive-preferred promoter may be isolated.

As used herein, promoter is intended to mean a nucleic acid, preferably DNA, that binds RNA polymerase and/or other transcription regulatory elements. As with any promoter, the promoters of the current invention will facilitate or control the transcription of DNA or RNA to generate an mRNA molecule from a nucleic acid molecule that is operably linked to the promoter. As stated earlier, the RNA generated may code for a protein or polypeptide or may code for an RNA interfering, or antisense molecule. As used herein, “operably linked” refers to the chemical fusion, ligation, or synthesis of DNA such that a promoter-nucleic acid sequence combination is formed in a proper orientation for the nucleic acid sequence to be transcribed into an RNA segment. The promoters of the current invention may also contain some or all of the 5′ untranslated region (5′ UTR) of the resulting mRNA transcript. On the other hand, the promoters of the current invention do not necessarily need to possess any of the 5′ UTR.

A promoter, as used herein, may also include regulatory elements. Conversely, a regulatory element may also be separate from a promoter. Regulatory elements confer a number of important characteristics upon a promoter region. Some elements bind transcription factors that enhance the rate of transcription of the operably linked nucleic acid. Other elements bind repressors that inhibit transcription activity. The integrated effect of transcription factors on promoter activity may determine whether the promoter activity is high or low, i.e. whether the promoter is “strong” or “weak.” Transcription factors that bind regulatory elements may themselves be regulated by the interaction with other bound proteins or by covalent modification, e.g. phosphorylation, in response to extracellular stimuli. The activity of some transcription factors is modulated by signaling molecules, such as intracellular metabolites or chemicals exogenous to the organism that communicate with the cellular nucleus. Promoters that are unaffected by changes in the cellular environment are referred to as constitutive promoters.

In another embodiment, the nucleic acids of the invention encode expression products that disrupt the metabolism, function, and/or development of the cell in which the nucleic acid is expressed. In one embodiment, the nucleic acids of the invention encode a cytotoxic expression product. In one embodiment, the nucleic acids of the invention embrace barnase. In a further embodiment, the barnase may be mutated by methods known in the art for increasing and/or decreasing barnase activity. In one embodiment, a mutated barnase may have attenuated cytotoxic activity.

The present invention also provides vectors comprising the isolated nucleic acid molecules and polypeptides of the invention. In one embodiment, the vectors of the present invention are Ti-plasmids derived from the A. tumefaciens.

In developing the constructs of this invention, the various components of the construct or fragments thereof will normally be inserted into a convenient cloning vector, e.g., a plasmid that is capable of replication in a bacterial host, e.g., E. coli. Numerous vectors exist that have been described in the literature, many of which are commercially available. After each cloning, the cloning vector with the desired insert may be isolated and subjected to further manipulation, such as restriction digestion, insertion of new fragments or nucleotides, ligation, deletion, mutation, resection, etc. to tailor the components of the desired sequence. Once the construct has been completed, it may then be transferred to an appropriate vector for further manipulation in accordance with the manner of transformation of the host cell.

A recombinant DNA molecule of the invention typically includes a selectable marker so that transformed cells can be easily identified and selected from non-transformed cells. Examples of such markers include, but are not limited to, a neomycin phosphotransferase (nptII) gene, which confers kanamycin resistance. Potrykus et al., Mol. Gen. Genet. 199:183-188 (1985). Cells expressing the nptII gene can be selected using an appropriate antibiotic such as kanamycin or G418. Other commonly used selectable markers include the bar gene, which confers bialaphos resistance; a mutant EPSP synthase gene (Hinchee et al., Bio/Technology 6:915-922 (1988)), which confers glyphosate resistance; a nitrilase gene, which confers resistance to bromoxynil (Stalker et al. J. Biol. Chem. 263:6310-6314 (1988)); a mutant acetolactate synthase gene (ALS), which confers imidazolinone or sulphonylurea resistance (European Patent Application 154,204, 1985); and a methotrexate resistant DHFR gene (Thillet et al. J. Biol. Chem. 263:12500-12508 (1988)).

Additionally, vectors may include an origin of replication (replicons) for a particular host cell. Various prokaryotic replicons are known to those skilled in the art, and function to direct autonomous replication and maintenance of a recombinant molecule in a prokaryotic host cell.

The vectors will preferably contain selectable markers. Numerous selectable markers for use in selecting transfected plant cells including, but not limited to, kanamycin, glyphosate resistance genes, and tetracycline or ampicillin resistance for culturing in E. coli, A. tumefaciens and other bacteria.

A plasmid vector suitable for the introduction of nucleic acid of the current invention into monocots using microprojectile bombardment is composed of the following: the promoter of choice; an intron that provides a splice site to facilitate expression of the gene, such as the Hsp70 intron (PCT Publication WO 93/19189); and a 3′ polyadenylation sequence such as the nopaline synthase 3′ sequence (NOS 3′). Fraley et al. Proc Natl Acad Sci USA 80: 4803-4807 (1983). This expression cassette may be assembled on high copy replicons suitable for the production of large quantities of DNA.

A particularly useful Agrobacterium-based plant transformation vector for use in transformation of dicotyledonous plants is plasmid vector pMON530 (Rogers et al. (1987) Improved vectors for plant transformation: expression cassette vectors and new selectable markers. In Methods in Enzymology. Edited by R. Wu and L. Grossman. p253-277. San Diego: Academic Press). Plasmid pMON530 is a derivative of pMON505 prepared by transferring the 2.3 kb StuI-HindIII fragment of pMON316 (Rogers et al. (1987) Improved vectors for plant transformation: expression cassette vectors and new selectable markers. In Methods in Enzymology. Edited by R. Wu and L. Grossman. p253-277. San Diego: Academic Press) into pMON526. Plasmid pMON526 is a simple derivative of pMON505 in which the SmaI site is removed by digestion with XmaI, treatment with Klenow polymerase and ligation. Plasmid pMON530 retains all the properties of pMON505 and the CaMV35S-NOS expression cassette and now contains a unique cleavage site for SmaI between the promoter and polyadenylation signal.

Binary vector pMON505 is a derivative of pMON200 (Rogers et al., 1987) in which the Ti plasmid homology region, LIH, has been replaced with a 3.8 kb HindIII to SmaI segment of the mini RK2 plasmid, pTJS75 (Schmidhauser and Helinski. J. Bacteriol. 164-155 (1985). This segment contains the RK2 origin of replication, oriV, and the origin of transfer, oriT, for conjugation into Agrobacterium using the tri-parental mating procedure (Horsch and Klee Proc. Natl. Acad. Sci. USA 83:4428-4432 (1986). Plasmid pMON505 retains all the important features of pMON200 including the synthetic multi-linker for insertion of desired DNA fragments, the chimeric NOS/NPTII′/NOS gene for kanamycin resistance in plant cells, the spectinomycin/streptomycin resistance determinant for selection in E. coli and A. tumefaciens, an intact nopaline synthase gene for facile scoring of transformants and inheritance in progeny, and a pBR322 origin of replication for ease in making large amounts of the vector in E. coli. Plasmid pMON505 contains a single T-DNA border derived from the right end of the pTiT37 nopaline-type T-DNA. Southern blot analyses have shown that plasmid pMON505 and any DNA that it carries are integrated into the plant genome, that is, the entire plasmid is the T-DNA that is inserted into the plant genome. One end of the integrated DNA is located between the right border sequence and the nopaline synthase gene and the other end is between the border sequence and the pBR322 sequences.

Another particularly useful T_(i) plasmid cassette vector is pMON17227. This vector is described in PCT Publication WO 92/04449 and contains a gene encoding an enzyme conferring glyphosate resistance (denominated CP4), which is an excellent selection marker gene for many plants, including potato and tomato. The gene is fused to the Arabidopsis EPSPS chloroplast transit peptide (CTP2), and expression is driven by the promoter of choice.

For secretion of the translated protein into the lumen of the endoplasmic reticulum, the periplasmic space or into the extracellular environment, appropriate secretion signals may be incorporated into the expressed polypeptide. The signals may be endogenous to the polypeptide or they may be heterologous signals.

In one embodiment, the vectors of the current invention are designed in a manner such that the nucleic acids described herein are tissue-specific promoters which are operably linked to DNA encoding a polypeptide of interest. In another embodiment, the polypeptide of interest is a protein involved in an aspect of reproductive development or regulating reproductive development. Polynucleotides encoding many of the proteins involved in reproductive development include, but are not limited to, AGAMOUS (AG), APETALA1 (AP1), APETAL3 (AP3), PISTILLATA (Pt), LEAFY (LFY), and LEUNIG (LUG).

In another embodiment, the coding sequence operably linked to a promoter may code for a gene product that inhibits the expression or activity of proteins involved in reproductive development. For example, a gene encoding the enzyme callase, which digests the callose cell wall surrounding the developing pollen grains, could be operably linked to a tapetum-preferred promoter and expressed before pollen maturation, thereby disrupting pollen development.

In another embodiment, the coding sequence operably linked to a promoter may encode a cytotoxic gene product. For instance, a gene encoding barnase may be operably linked to a reproductive-preferred promoter and expressed in a reproductive tissue. In a further embodiment, standard molecular biology methods may be used for mutating barnase activity. In one embodiment, a mutated barnase has reduced RNase activity compared with a wild type barnase protein. In a further embodiment, a mutated barnase having reduced RNase activity is operably linked to a reproductive-preferred promoter and expressed in a reproductive tissue. In a further embodiment, the expression of a mutated barnase having reduced RNase activity in a reproductive tissue does not compromise vegetative growth and development.

In a further embodiment, the vectors of the current invention are designed such that the nucleic acids of the current invention are operably linked to a nucleic acid encoding an antisense RNA or interfering RNA, which corresponds to a gene that code for a polypeptide of interest, resulting in a decreased expression of a targeted gene product. In one embodiment, the gene products targeted for suppression are proteins involved in reproductive development. The use of RNAi inhibition of gene expression is described generally in Paddison et al., Genes & Dev. 16: 948-958 (2002), and the use of RNAi to inhibit gene expression in plants is specifically described in WO 99/61631, both of which are herein incorporated by reference.

The use of antisense technology to reduce or inhibit the expression of specific plant genes has been described, for example in European Patent Publication No. 271,988. Reduction of gene expression led to a change in the phenotype of the plant, either at the level of gross visible phenotypic difference, for example a lack of lycopene synthesis in the fruit of tomato leading to the production of yellow rather than red fruit, or at a more subtle biochemical level, for example, a change in the amount of polygalacturonase and reduction in depolymerisation of pectins during tomato fruit ripening. Smith et. al., Nature, 334:724-726 (1988). Smith et. al., Plant Mol. Biol., 14:369-379 (1990). Thus, antisense RNA has been demonstrated to be useful in achieving reduction of gene expression in plants.

In one embodiment of the method of making a plant of the invention, an exogenous DNA capable of being transcribed inside a plant to yield an antisense RNA transcript is introduced into the plant, e.g., into a plant cell. The exogenous DNA can be prepared, for example, by reversing the orientation of a gene sequence with respect to its promoter. Transcription of the exogenous DNA in the plant cell generates an intracellular RNA transcript that is “antisense” with respect to that gene.

The invention also provides host cells which comprise the vectors of the current invention. As used herein, a host cell refers to the cell in which the coding product is ultimately expressed. Accordingly, a host cell can be an individual cell, a cell culture or cells as part of an organism. The host cell can also be a portion of an embryo, endosperm, sperm or egg cell, or a fertilized egg.

The vectors of the current invention are introduced into the host cells by standard procedures known in the art for introducing recombinant vector DNA into the target host cell. Such procedures include, but are not limited to, transfection, infection, transformation, natural uptake, electroporation, biolistics and Agrobacterium. Methods for introducing foreign genes into plants are known in the art and can be used to insert a gene construct of the invention into a plant host, including, biological and physical plant transformation protocols. See, for example, Miki et al., 1993, “Procedure for Introducing Foreign DNA Into Plants”, In: Methods in Plant Molecular Biology and Biotechnology, Glick and Thompson, eds., CRC Press, Inc., Boca Raton, pages 67-88. The methods chosen vary with the host plant, and include chemical transfection methods such as calcium phosphate, microorganism-mediated gene transfer such as Agrobacterium (Horsch et al., Science 227:1229-31, (1985)), electroporation, micro-injection, and biolistic bombardment.

Accordingly, the present invention also provides plants or plant cells, comprising the vectors of the current invention. In one embodiment, the plants are angiosperms or gymnosperms. In another embodiment, the plants are selected from Eucalyptus and its hybrids, and Pinus species. Alternatively, the plant may be selected from Pinus banksiana, Pinus brutia, Pinus caribaea, Pinus clasusa, Pinus contorta, Pinus coulteri, Pinus echinata, Pinus eldarica, Pinus ellioti, Pinus jeffreyi, Pinus lambertiana, Pinus massoniana, Pinus monticola, Pinus nigra, Pinus palustrus, pinus pinaster, Pinus ponderosa, Pinus radiata, Pinus resinosa, Pinus rigida, Pinus serotina, Pinus strobus, Pinus sylvestris, Pinus taeda, Pinus virginiana, Abies amabilis, Abies balsamea, Abies concolor, Abies grandis, Abies lasiocarpa, Abies magnifica, Abies procera, Chamaecyparis lawsoniona, Chamaecyparis nootkatensis, Chamaecyparis thyoides, Juniperus virginiana, Larix decidua, Larix laricina, Larix leptolepis, Larix occidentalis, Larix siberica, Libocedrus decurrens, Picea abies, Picea engelmanni, Picea glauca, Picea mariana, Picea pungens, Picea rubens, Picea sitchensis, Pseudotsuga menziesii, Sequoia gigantea, Sequoia sempervirens, Taxodium distichum, Tsuga canadensis, Tsuga heterophylla, Tsuga mertensiana, Thuja occidentalis, Thuja plicata, Eucalyptus alba, Eucalyptus bancroftii, Eucalyptus botryoides, Eucalyptus bridgesiana, Eucalyptus calophylla, Eucalyptus camaldulensis, Eucalyptus citriodora, Eucalyptus cladocalyx, Eucalyptus coccifera, Eucalyptus curtisii, Eucalyptus dalrympleana, Eucalyptus deglupta, Eucalyptus delagatensis, Eucalyptus diversicolor, Eucalyptus dunnii, Eucalyptus ficifolia, Eucalyptus grandis, Eucalyptus globulus, Eucalyptus gomphocephala, Eucalyptus gunnii, Eucalyptus henryi, Eucalyptus laevopinea, Eucalyptus macarthurii, Eucalyptus macrorhyncha, Eucalyptus maculata, Eucalyptus marginata, Eucalyptus megacarpa, Eucalyptus melliodora, Eucalyptus nicholii, Eucalyptus nitens, Eucalyptus nova-angelica, Eucalyptus obliqua, Eucalyptus occidentalis Eucalyptus obtusiflora, Eucalyptus oreades, Eucalyptus pauciflora, Eucalyptus polybractea, Eucalyptus regnans, Eucalyptus resinifera, Eucalyptus robusta, Eucalyptus rudis, Eucalyptus saligna, Eucalyptus sideroxylon, Eucalyptus stuartiana, Eucalyptus tereticornis, Eucalyptus torelliana, Eucalyptus urnigera, Eucalyptus urophylla, Eucalyptus viminalis, Eucalyptus viridis, Eucalyptus wandoo, and Eucalyptus youmanni. In particular, the transgenic plant may be of the species Eucalyptus grandis, Pinus radiata, Pinus taeda L (loblolly pine), Populus nigra, Populus deltoides, Tectona grandis, or Acacia mangium.

Beyond the ordinary meaning of plant, the term “plants” is also intended to mean the fruit, seeds, flower, strobilus etc. of the plant. The plant of the current invention may be a direct transfectant, meaning that the vector was introduced directly into the plant, such as through Agrobacterium, or the plant may be the progeny of a transfected plant. The second or subsequent generation plant may or may not be produced by sexual reproduction, i.e., fertilization. Furthermore, the plant can be a gametophyte (haploid stage) or a sporophyte (diploid stage).

The present invention also provides a method for controlling reproductive development in a plant comprising cultivating a plant or seed comprising the vectors of the current invention. Proper cultivation to induce or sustain the growth or germination of the plants or seeds of the current invention is species-specific, and within the level of ordinary skill in the art. The setting for cultivation may be anywhere which fosters the growth or germination of the plant or seed. Furthermore, cultivation can also include steps such as, but not limited to, providing a stress treatment, (e.g., nitrogen deprivation, heat shock, low temperatures, sucrose deprivation) which can induce embyrogenesis.

The invention further provides isolated regulatory elements that bind transcription factors and are capable of regulating tissue-preferred or tissue-specific expression. The degree of regulation conferred by the regulatory elements may be complete, meaning that transcription is not detectable without the transcription factors, or partial, meaning that transcription is enhanced in the presence of the transcription factors. In one embodiment, at least one regulatory element is operably linked to a heterologous promoter to provide a composite promoter. The composite promoter is expressed preferentially or specifically in reproductive tissue. As used herein, heterologous promoters is a phrase whose meaning term that is relative to the regulatory elements. If a regulatory element and a promoter do not associate with one another in a natural setting, the promoter would be considered heterologous to the regulatory element. Typically, the precise orientation of a regulatory element within a promoter region will not affect its activity. Furthermore, regulatory elements can function normally when inserted into heterologous promoter regions. Thus, for example, reproductive-preferred regulatory elements can be removed from their endogenous promoter and can be inserted into heterologous promoter regions to confer reproductive-specificity or preference. The heterologous promoter may be, for example, a minimal CaMV 35S promoter. Promoters that direct expression in plant cells which are suitable for modification to minimal promoters include the cauliflower virus (CaMV) 35S promoter (Jefferson et al., EMBO J., 6: 3901-07 (1987)), the rice actin promoter (McElroy et al., Plant Cell, 2: 163-71 (1990)), the maize ubiquitin-1 promoter (Christensen et al., Transgenic Research, 5: 213-18 (1996)), and the nopaline synthase promoter (Kononowics et al., Plant Cell 4: 17-27 (1992)).

To prepare the nucleic acids of the invention, genomic libraries were made from Pinus radiata and Pinus taeda, using a variety of restriction endonucleases to digest the genome into discrete fragments. Genomic libraries can be similarly constructed from any plant species from which it is desirable to obtain tissue-selective promoters. An adaptor was ligated to each of these genomic sequences, according to the procedure provided by Clontech for use of its GenomeWalker™ Systems (Clontech, Palo Alto, Calif.). Promoter sequences then were PCR-amplified using adaptor-specific primers and “gene-specific primers.” Alternatively, this PCR amplification step optionally may be conducted by the methodology described in U.S. Pat. No. 5,565,340 and No. 5,759,822, herein incorporated by reference, to yield reaction products of long length and minimal background. Using this general PCR amplification methodology, the identification of the promoter of the invention and its identification as a tissue-selective promoter, is governed by the choice of the “gene-specific primer.”

A gene-specific primer is any transcribed sequence that is expressed at high levels in a tissue of interest. In the present invention, the gene-specific primer is a fragment of, or is complementary to, an mRNA that is expressed at high levels in reproductive tissue. In one embodiment, the gene-specific primer is selected by its homology to genes that are known to be expressed specifically in a particular reproductive tissue type. Genes of particular interest are those that are expressed in a particular reproductive tissue at high levels, which typically is an indicator of reproductive-preferred activity of the corresponding promoter.

Expressed sequence tags (ESTs) provide another source of gene-specific primers. An EST is a cDNA fragment of a corresponding mRNA that is present in a given library. Any plant EST database may be searched electronically to find ESTs that share identity to segments of genes that are known to be expressed specifically in a desired tissue type (“in silico screening”). These ESTs thus will provide gene-specific primers for the amplification of the promoter of the corresponding gene in a given genomic library. The amplified gene promoter need not be from the same species from which the EST database was obtained. All that is required is that the EST bears sufficient sequence similarity to the gene promoter of interest to act as a primer for PCR amplification of the target segment of the gene.

An alternative methodology to identify tissue-specific promoters rests on detection of mRNAs that are expressed in one tissue type, but not in another, implying that they are transcribed from a tissue-specific promoter. Populations of mRNAs can be distinguished on this basis by subtractive hybridization, for example. One such suitable subtractive hybridization technique is the PCR-Select™ described by Clontech.

Alternatively, a tissue-specific mRNA distribution can be determined by in situ hybridization of thin slices of plant tissue with radiolabeled probes. Probes that radioactively stain a particular tissue type are then used to detect the promoter associated with the mRNA by Southern analysis of genomic libraries, using the methodologies described below. All of the aforementioned techniques require the preparation of mRNA libraries from the tissue of interest, in this case, reproductive tissue. cDNA libraries may be made from reproductive tissues isolated from woody plant species. For example, male and female buds were isolated from P. radiata and P. taeda. Briefly, total RNA is isolated using standard techniques, and poly(A) RNA then is isolated and reverse transcribed to construct a reproductive-preferred tissue cDNA library. The cDNA library may be constructed in the λZAP-XR vector, employing Strategene cDNA synthesis and Gigapakll Gold™ packaging kits. Reproductive-specific promoters can, in turn, be isolated from such cDNA libraries by PCR using a gene-specific probe and a primer that recognizes a sequence at the 5′ end of the promoter. A gene-specific probe can be obtained by the in silico approach described above, or by designing a specific probe based on the sequence of the mRNA, if known. Furthermore, a primer can be synthesized which is complementary to the 5′ UTR of the desired target gene. Alternatively, the primer can be designed from a partial amino acid sequence of the encoded protein, as a so-called degenerate primer.

Following isolation of the promoter of interest, various methods can be used to characterize its tissue-specific expression pattern and promoter strength. One commonly employed method is to operably link the promoter to a readily assayed reporter gene. For example, a reproductive-preferred promoter has been operably linked to the gene encoding β-glucuronidase (GUS). Lacombe et al., Plant J. 23: 663-76 (2000). Suitable expression constructs can be made using well-known methodologies.

Transformation of plants can be accomplished by any one of many suitable techniques, including Agrobacterium-mediated transformation, as described in U.S. Pat. No. 6,051,757. Other methods for transforming trees are known in the art, as exemplified by U.S. Pat. No. 5,681,730, which discloses an accelerated particle transformation method of gymnosperm somatic embryos. Other transformation methods include micro-projectile bombardment (Klein et al., Biotechnology 6: 559-63 (1988)), electroporation (Dhalluin et al., Plant Cell 4: 1495-1505 (1992)), and polyethylene glycol treatment (Golovkin et al., Plant Sci. 90: 41-52 (1993)). Further, U.S. Pat. No. 6,187,994 discloses a recombinase-assisted insertion of the expression construct into a specific, selected site within a plant genome. All of the aforementioned patents and publications are herein incorporated by reference.

A DNA molecule of the present invention can be inserted into the genome of a plant by any suitable method. Suitable plant transformation vectors include those derived from a Ti plasmid of Agrobacterium tumefaciens, as well as those disclosed, e.g., by Herrera-Estrella et al. Nature 303:209 (1983), Bevan Nucleic Acids Res. 12 (22): 8711-8721 (1984), Klee et al. Bio/Technology 3(7): 637-642 (1985) and European Patent publication 120,516. In addition to plant transformation vectors derived from the Ti or root-inducing (Ri) plasmids of Agrobacterium, alternative methods can be used to insert the DNA constructs of this invention into plant cells. Such methods may involve, for example, the use of liposomes, electroporation, chemicals that increase free DNA uptake, free DNA delivery via microprojectile bombardment, and transformation using viruses or pollen. DNA may also be inserted into the chloroplast genome (Daniell et al. Nature Biotechnology 16:345-348 (1998)).

When adequate numbers of cells (or protoplasts) containing the nucleic acid of interest are obtained, the cells (or protoplasts) are regenerated into whole plants. Choice of methodology for the regeneration step is not critical, with suitable protocols being available for hosts from Leguminosae (alfalfa, soybean, clover, etc.), Umbelliferae (carrot, celery, parsnip), Cruciferae (cabbage, radish, canola/rapeseed, etc.), Cucurbitaceae (melons and cucumber), Gramineae (wheat, barley, rice, maize, etc.), Solanaceae (potato, tobacco, tomato, peppers), various reproductive crops, such as sunflower, and nut-bearing trees, such as almonds, cashews, walnuts, and pecans. See, e.g., Ammirato et al. (1984) Handbook of Plant Cell Culture-Crop Species. Macmillan Publ. Co.; Fromm, M., (1990) UCLA Symposium on Molecular Strategies for Crop Improvement, Apr. 16-22, 1990. Keystone, Colo.; Vasil et al. Bio/Technology 8:429-434 (1990); Vasil et al. Bio/Technology 10:667-674 (1992); Hayashimoto et al. Plant Physiol. 93:857-863 (1990); and Datta et al. (1990).

The vector comprising the promoter and reporter gene includes a mechanism to select those plant cells successfully transformed with the vector, which may be, for example, kanamycin resistant. The presence of the GUS gene in transformants may be confirmed by a PCR approach, using GUS-specific PCR primers (Clontech, Palo Alto). Segregation of kanamycin resistance in the progeny of the transformed plant cells can be used in conjunction with Southern analysis to determine the number of loci harboring the stably inserted vector. The temporal and spatial pattern of promoter expression is then inferred from a quantification of the reporter gene expression, as described in Jefferson et al., EMBO J. 6: 3901-07 (1987). Generally, GUS expression is determined histochemically in thin slices of plant tissues that are fixed first in 90% acetone and then in a buffered solution containing a GUS substrate, 5-bromo-4-chloro-3-indoyl-β-D-glucuronic acid (X-Gluc). The presence of the GUS expression product is indicated by a calorimetric reaction with the X-Gluc.

Reproductive-specific expression, for example, can be conferred by the presence of regulatory elements that specifically bind transcription factors in reproductive tissue. The interaction between reproductive-specific regulatory elements and reproductive-preferred transcription factors depends on the alignment between a subset of base pairs of the regulatory element with amino acid residues of the transcription factor. Likewise, tapetum-specific expression, for example, can be conferred by the presence of regulatory elements that specifically bind transcription factors in tapetal tissue. Base pairs that do not interact with the bound transcription factor may be substituted with other base pairs, while maintaining the overall ability of the regulatory element to bind specifically the tissue-specific transcription factor.

Various methodologies can be used to identify and characterize regulatory elements that affect tissue-preferred or tissue-specific promoter activity, once a promoter is identified as tissue-preferred or specific. In one methodology, the promoter region is sequentially truncated at the 5′ end and the series of truncated promoters are each operably linked to a reporter gene. When a regulatory element is deleted, the effect on the promoter activity is inferred by the loss of tissue-specific expression of the reporter gene. Alternatively, a putative regulatory element can be inserted into an expression construct containing a minimal promoter, such as the CaMV 35S minimal promoter (Keller et al., Plant Mol. Biol. 26: 747-56) to ascertain if the putative regulatory element confers tissue-specific expression. A minimal promoter contains only those elements absolutely required for promoter activity, such as a RNA polymerase binding site. Additional examples for elucidating putative regulatory elements are provided by studies of tissue-specific regulatory elements that coordinately regulate transcription of the genes encoding L-phenyl-alanine ammonia-lyase (PAL) and 4-coumarate CoA ligase (4CL). Hatton et al., Plant J. 7: 859-76 (1995); Leyva et al., Plant Cell 4: 263-71 (1992); Hauffe et al., Plant J. 4: 235-53 (1993); Neustaedter et al., Plant J. 18: 77-88 (1999), all of which are incorporated herein by reference.

Functional Variants or Fragments of the Promoters of the Invention

Additional variants or fragments of the promoters of the invention are those with modifications interspersed throughout the sequence. Functional variants or fragments, as used herein, are nucleic acids that have a nucleic acid sequence at least about 70% identical to the reference nucleic acid, but still confer tissue-specific expression of coding products. The tissue-specificity or preference of the functional variant must be towards the same tissue as the reference nucleic acid. However, even if the functional variant is not as preferential or as specific as the reference nucleic acid, the variant is still considered a functional variant as used herein. In one embodiment, the sequence of the functional variant or fragment is at least about 75% identical to the reference nucleic acid. In other embodiments, the sequence of the functional variant or fragment is at least about 80%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99%.

Modifications that can produce functional variants may be made by sequential deletion of residues from the 5′ end or the deletion of 5′ UTR sequences from the 3′ end. Alternatively, internal residues may be modified. Modifications that do not affect the function of the promoter regions most likely will be those that do not affect the binding of transcription factors. The modifications encompassed by the invention also include those that occur naturally in the form of allelic variants of the promoters of the invention.

Methods of Making the Nucleic Acids of the Present Invention

The nucleic acids of the invention can be obtained by using well-known synthetic techniques, standard recombinant methods, purification techniques, or combinations thereof. For example, the isolated polynucleotides of the present invention can be prepared by direct chemical synthesis using the solid phase phosphoramidite triester method (Beaucage et al., Tetra. Letts. 22: 1859-1862 (1981)), an automated synthesizer (Van Devanter et al., Nucleic Acids Res. 12: 6159-6168 (1984)), or the solid support method of U.S. Pat. No. 4,458,066. Chemical synthesis generally produces a single stranded oligonucleotide, which can be converted into double stranded oligonucleotides by hybridization with a complementary sequence, or by polymerization, using the single strand as a template. Also, longer sequences may be obtained by the ligation of shorter sequences.

Alternatively, the nucleic acids of the present invention can be obtained by recombinant methods using mutually priming oligonucleotides. See e.g. Ausubel et al., (eds.), CURRENT PROTOCOLS IN MOLECULAR BIOLOGY (John Wiley & Sons, Inc. 1990). Also, see Wosnick et al., Gene 60: 115 (1987); and Ausubel et al. (eds.), SHORT PROTOCOLS IN MOLECULAR BIOLOGY, 3^(rd) ed., (John Wiley & Sons, Inc. 1995). Established techniques using the polymerase chain reaction provide the ability to synthesize polynucleotides at least 2 kilobases in length. Adang et al., Plant Mol. Biol. 21: 1131 (1993); Bambot et al., PCR Methods and Applications 2: 266 (1993); Dillon et al., “Use of the Polymerase Chain Reaction for the Rapid Construction of Synthetic Genes,” in METHODS IN MOLECULAR BIOLOGY, Vol. 15: PCR PROTOCOLS: CURRENT METHODS AND APPLICATIONS, White (ed.), pages 263-268, (Humana Press, Inc. 1993); Holowachuk et al., PCR Methods Appl. 4: 299 (1995).

Methods of Using the Nucleic Acids of the Invention

The nucleic acids of the current invention are useful for altering characteristics of a plant. The nucleic acids may be operably linked to a gene of interest to increase the levels of a molecule found in the reproductive tissue. Alternatively, the gene of interest may inhibit reproductive development, thereby conferring sterility to a plant.

One of the primary targets of such manipulated expression is reproductive development. For the reasons set forth above, there is considerable interest in regulating reproductive development, accomplished through genetic ablation. For example, a cytotoxic barnase molecule under the control of a tapetum-preferred promoter has been used for regulating reproductive development. European Patent Publication 344, 029.

For example, a mutant barnase gene having reduced RNase activity may be used for regulating reproductive development. In one embodiment, the mutant barnase gene may be operably linked to a promoter such that expression of the barnase gene could impose little or no damage to vegetative tissues, yet the mutant barnase may provide adequate RNase activity for reproductive ablation.

The present invention, thus generally described, will be understood more readily by reference to the following examples, which are provided by way of illustration and are not intended to be limiting of the present invention.

EXAMPLES Example 1 Isolation of Reproductive-Preferred Promoters

Reproductive-preferred plant promoters can be isolated from genomic and cDNA libraries. Using the sequence of a reproductive-preferred promoter as a probe, putative reproductive-preferred promoter sequences can be isolated. For example, an AGAMOUS (AG) promoter from P. radiata may be used as a probe for identifying other reproductive-preferred promoter sequences.

For example, genomic DNA was isolated from a male-bud from loblolly pine. Following isolation of the male-bud DNA, the P. radiata AG1 sequence was used as a probe for screening the male-bud genomic DNA isolated. Using a PCR-based screening approach, two putative loblolly pine AG promoter sequences were isolated, denoted LPAG1(SEQ ID NO: 1) and LPAG2 (SEQ ID NO: 2). Each cloned LPAG promoter is about 1400 bp, including 600 bp of 5′ untranslated region, which contains the first intron of 139 bp of LPAG1 or LPAG2 gene.

The promoters were cloned using a “Genome Walker” kit (Clontech, Palo Alto, Calif.). This is a PCR-based method, which requires four PCR primers to be constructed, two of which must be gene-specific. The gene specific primers are designed generally within the 5′ UTR of the gene. The fragment is amplified and then cloned into a T-tailed vector in front of the GUS reporter gene.

Example 2 Methodology to Determine the Tissue Specificity of a Promoter

Following the identification and cloning of a promoter as described in Example 1, the promoter is operably linked with a reporter gene to determine those tissue types in which the promoter is active. To this end, a construct containing an inventive promoter is transformed into Agrobacterium tumefaciens by electroporation. Briefly, 40 μl of diluted AgL-1 competent cells are placed on ice and are contacted with about 10 ng of pART27 vector containing the promoter sequence. Electroporation is conducted under the following parameters:

-   -   Resistance=129 ohm     -   Charging voltage=1.44 kV     -   Field strength=14.4 kV/cm     -   Pulse duration=5.0 ms

Following electroporation, 400 μl of YEP liquid media is added and the cells are allowed to recover for one hour at room temperature. Cells then are centrifuged at 6000 rpm for 3 min and are resuspended in ˜50 μl YEP. Cell samples are spread over the surface of a YEP Kan50/Rif50 plate, sealed with parafilm, and incubated at 29° C. for 2 days for colony growth.

Tobacco (Nicotiana tabacum) plants are transformed with constructs of interest by Agrobacterium-mediated leaf tissue transformation (Burow et al., Plant Mol. Biol. Rep. 8:124-139, 1990).

Successfully transformed plants are then assayed for the expression of the operably linked reporter gene. Leaf, stem, root and reproductive regions are immersed in a staining solution (50 mM NaPO₄, pH 7.2, 0.5% Triton X-100, 1 mM X-Glucuronide, cycloheximide salt (Ducheffa). A vacuum is applied twice for 5 min to infiltrate the tissue with the staining solution. The tissue is then left shaking overnight at 37° C. for color development. Tissues are checked at three or four time-points to check stain development, and if samples show early development, a piece of tissue is destained in 70% ethanol.

The GUS localization, as shown in Table 1, demonstrate that the disclosed isolated nucleotide sequences confer reporter gene expression preferentially in reproductive tissues, such as the tapetum.

As shown in Example 6, expression of a reproductive-preferred promoter is expected in vegetative tips in the presence of the primary inflorescence when the vegetative growth of axilliary buds is suppressed and the transition from vegetative buds and reproductive buds is fast.

TABLE 1 In planta GUS reproductive expression GUS Reproductive No. of Plants % GUS Localization in GUS Reproductive SEQ ID NO GUS + Expression Tobacco Localization in Pine 1 LPAG1 15 Tobacco 93 Tobacco Petals, Stamens, Embryogenic calli 17 Pine 70 Pine Carpels, and regenerated Vegetative Shoot embryo Tip 2 LPAG2 7 Tobacco 64 Tobacco Petals, Stamens, Embryogenic calli 6 Pine 40 Pine Carpels, and regenerated Vegetative Shoot embryo Tip 3 PrAG 1 Tobacco 5.2 Tobacco NO GUS staining Embryogenic calli 28 Pine 78 Pine and regenerated embryo 4 PrMC2 24 Tobacco 100 Tobacco Anthers, Tapetum No GUS staining in 400-1 Embryogenic calli and regenerated embryo 16 PrMC2 11 (Tobacco) 91 (Tobacco) Anthers, Tapetum No GUS staining in 400-3 2 (Pine) 12.5 (Pine) Embryogenic calli and regenerated embryo

As described in more detail below, the “PRMC2” promoter constructs comprise a reproductive-preferred promoter from P. radiata operably linked to a barnase mutant, specifically H102E for PrMC2.400-1 and PrMC2.400-3. GUS expression has not been observed in anthers of tobacco transformed with the PrMC2.400 promoter. Accordingly, an in-frame PrMC2.400 promoter was cloned for use in an ablation construct and used in the experiments described above.

Example 3 Methods of Using a Reproductive-Specific Promoter

Once a promoter having an appropriate tissue-specific and developmental pattern of expression is found, this promoter can be used to regulate a desired characteristic in a transgenic plant. In one embodiment, a tapetum-preferred promoter is used for regulating reproductive development in a plant. In this example, a tapetum-preferred promoter of the invention is operably linked to a gene encoding a cytotoxic protein. For example, a tapetum-preferred promoter may be operably linked to a gene encoding barnase. Expression of barnase in a reproductive-preferred tissue, such as the tapetum, may result in pollen ablation. European Patent Publication 344, 1990.

To construct a transgenic plant having ablated male reproductive development, a fragment of barnase cDNA is operably linked in proper orientation to a reproductive-specific promoter of the invention and a nopaline synthase 3′ terminator. The entire construct is inserted as a restriction fragment into the binary vector pBI101.1 (Clontech, Palo Alto, Calif.). Vectors are electroporated into A. tumefaciens strain LBA4404 or C58 pMP90, for tobacco or poplar transformations, respectively. See generally, No et al., Plant Science 160: 77-86 (2000). A tobacco leaf disc, as described above, or a poplar stem section, is dipped into the Agrobacterium culture as described above, according to the procedure of Leple et al., Plant Cell Rep. 11: 137-141 (1992). Kanamycin-resistant transformants are tested for activity, transgene copy number is determined by Southern analysis, and suitable transformants are rooted and transferred to a greenhouse.

Example 4 Method for Producing and Selecting an Attenuated Cytotoxic Enzyme

Synthesis of Barnase E73G and Barnase F106S

The barnase mutants F106S and E73G were obtained by random PCR mutagenesis. The PrAG promoter was operably linked to wild-type barnase coding region and three PCR reactions were performed such that the PrAG translation start codon ATG was replaced by barnase translation codon. In the first PCR, the 5′ primer, PrAGKpn (5′-GGTTTGGTACCTAACTTGCC-3′, SEQ ID NO: 27), anneals to the −199 to −179 positions of the PrAG promoter in reference to its translation starting ATG position, while the 3′ primer, PrAG-7:

(5′-CGTGTTGATAACCTGTGCCATGATTTGTACACAAAATTTCCG-3, SEQ ID NO: 28′)

anneals to the −21 to +3 positions including the translation starting ATG. The PrAG-7 primer has extra 18 bases which is complementary to the 5′ of the barnase coding region. The PCR mixture contains 50 ng of the template DNA (pWVCZ3 DNA), 200 □M of dNTPs, 1.5 mM of MgCl₂, and 0.5 □l of Taq DNA polymerase (Perkin Elmer). The DNA is denatured at 95° C. for 20 seconds, reannealed at 55° C. for 30 seconds, and incubated at 72° C. for 60 seconds. This PCR cycle was repeated 25 times. Following PCR, a 220 bp product was gel-purified.

In the second PCR, the 5′ primer, PrAG-8:

(5′-CGGAAATTTTGTGTACAAATCATGGCACAGGTTATCAACACG-3′, SEQ ID NO: 29)

anneals to the 5′ of the barnase coding region, and this primer has 21 extra bases which are complementary to the 3′ of the PrAG promoter. The 3′ primer, 3Barn (GGTTCTCGAGTTTCACGTTAACTGGCTAG), anneals to the 3′ of the barnase DNA and carries a Sac I site for cloning. The PCR mixture contains 50 ng of the template DNA (pWVR14), 200 μM of dNTPs, 1.5 m, SEQ ID NO: 30M of MgCl₂, and 0.5 μl of Taq DNA polymerase (Perkin Elmer). The DNA is denatured at 95° C. for 20 seconds, reannealed at 55° C. for 30 seconds, and incubated Oat 72° C. for 60 seconds. This PCR cycle was repeated 25 times. Following PCR, a 462 bp product is gel-purified.

In the third PCR, the 5′ primer is the PrAGKpn and the 3′ primer is 3Barn, and the DNA template is the mixture of the equal amount of the first and the second PCR products (˜40 ng each). The amplified product of the third PCR is 640 bp which is the fusion between the 3′ of the PrAG promoter and the barnase coding region. After the third PCR, the PCR fragment was digested with Kpn I and Sac I and ligated to the plasmid (pUC19) which already carries the PrAG promoter so that after the ligation the barnase is driven by the full-length of the PrAG promoter.

The ligation mixture was introduced into E. coli by electroporation and transformed colonies were grown on LB agar containing 75 ug/ml ampicillin. Plasmids were extracted from two colonies and restriction enzyme digestion confirmed the presence of PrAG::barnase inserts. The plasmid DNAs were sequenced to confirm that they all have a mutation in the barnase coding region.

It was realized that all of the colonies growing on the LB plates contain mutant forms of barnase, and most of the mutations abolished barnase activity. However, some of the mutations decreased barnase activity, as indicated by the smaller sizes of colonies on the LB plates. About 100 colonies were selected and inoculated into 1 ml of LB liquid containing 75 ug/mL ampicillin. Following overnight culture at 37° C., the cell densities of the cultures were compared, and five cultures with significantly lower cell densities were selected. Low cell density indicates that the barnase is active, but much less toxic. The plasmids were purified from the five E. coli cultures and reintroduced into E. coli to confirm that the introduced plasmids, indeed, cause the smaller size of colonies on the LB agar plates, suggesting attenuated barnase activity carried by the plasmids. The reintroduction of the plasmids into E. coli was repeated three times. The confirmed plasmids were sequenced, and the results showed that the plasmid extracted from E. coli culture 29-S contained a single nucleotide substitution (A→G) in the codon for glutamate at position 73 of the barnase coding region, leading to the change of the glutamate for glycine. This barnase mutant was named barnase E73G (SEQ ID NO. 11). The plasmid extracted from E. coli culture 43-S also contained a single nucleotide substitution (T→C) in the codon for phenylalanine at position 106 of the barnase coding region, leading to the change of phenylalanine for serine. This barnase mutant was named barnase F106S (SEQ ID NO. 12).

Barnase F106S Assay

To assay F106S toxicity, tobacco plants were transformed, as described above in Example 2, with a construct having the PrAG promoter operably linked to a gene encoding mutant barnase F106S. No viable tobacco transformants were produced, as expression of mutant barnase F106S was lethal. These results indicate that there is a need for an attenuated barnase that, for example, can induce male-sterility, without adversely affecting vegetative growth.

Barnase E73G Assay

The barnase mutant E73G was selected for reproductive ablation based on the results of toxicity screening in E. coli. Expression of barnase E73G in E. coli resulted in a low level of toxicity. Specifically, barnase E73G inhibited E. coli growth in LB liquid medium and on LB solid plates. Although the value of reduced RNase activity (toxicity) of the barnase mutants can not be obtained from this biological screen, these results suggest that E73G has attenuated RNase activity.

Further evidence for attenuated barnase activity in barnase E73G may be found in a comparison study between barnase E73G and F106S. In a comparison, barnase F106S caused significantly more E. coli toxicity than barnase E73G. These results suggest that barnase F106S has higher RNase activity than barnase E73G.

Barnase H102E

The barnase H102E mutation was selected based upon a report that the corresponding mutation in a related enzyme, binase, had approximately 2% of the activity of the native enzyme. Yakovlev et al. FEBS Lett. 354: 305-306 (1994). As described below in Example 5, barnase H102E has attenuated activity. In this mutant, the codon for histidine 102 was substituted by a glutamate codon.

Directed mutagenesis of the barnase segment made use of an existing plasmid, pWVR14, that comprised the wild-type barnase coding region. This prior cloning of barnase used primers BAR5NCO (5′-TGACAACCATGGCACAGGTTATCAACACGTTTGAC-3, SEQ ID NO: 31′) and BAR3MFE (5′-AAAGTGCAATTGACCGATCAGAGTTTGAAG-3′, SEQ ID NO: 32) to amplify the entire coding region from the barnase cassette of plasmid pMT416. Hartley, R. W. J. Mol. Biol. 202: 913-915 (1988). The amplified fragment was digested with NcoI and cloned into a prepared vector with one NcoI end and one blunt end. The resulting plasmid, pWVR14, put the barnase segment adjacent to the promoter and 5′-UTR of the SEPALLATA1 gene (SEP1, previously called AGL2) and the mutagenesis procedure made use of the promoter sequence. Primers AGL2PB (5′-TTTCACAACCTCCACACACTT-3′, SEQ ID NO: 33) and BARH2E (5′-GTAAAGGTCTGATACTCGTCCGTTG-3′, SEQ ID NO: 34) were used to amplify the 5′ portion of the coding region plus a segment of the adjoining promoter. Primers BAR5NCO and BAR3MFE were used to amplify the wild-type barnase cassette. After amplification, the fragments were purified away from the primers and PCR reagents using gel electrophoresis and the QIAEX gel purification kit (QIAGEN). Approximately 100 ng of each fragment was combined with 1× Perkin Elmer Taq buffer, 1.6 mM MgCl₂, 0.10 mM each dNTP and 0.5 μl Perkin Elmer Taq DNA polymerase in a 50 μl reaction, and the mixture was repeatedly denatured at 95° C., reannealed at 50° C. and incubated at 72° C. (five cycles) in order to allow extension of the 0.75 kb fragment comprising a portion of the SEP1 promoter and the complete barnase coding region. The 0.75 kb fragment was further amplified by adding 10 μl of the extension reaction to a 50 μl mixture containing 20 μmol each of primers AGL2PB and BAR3MFE, 1×PCR buffer, 1.6 mM MgCl₂, 0.250 mM each dNTP and 0.5 μl Taq DNA polymerase, and running seven more cycles. The fragment was digested with NcoI, and the barnase segment was gel purified and ligated into a vector with NcoI and blunt ends. The correct mutation was verified by sequence analysis. For subsequent work, such as assembly of pWVR220, the full-length barnase H102E fragment was amplified using primers BAR5NCO and BAR3SAC (5′-GAAGAAGAGCTCTTGACCGATCAGAGTTTGAAG-3′, SEQ ID NO: 35), digested with NcoI and SacI, and purified. Because of the desire to have an NcoI site at the translation initation codon, an extra Alanine codon immediately after the ATG was included in primer BAR5NCO. This resulted in the His to Glu mutation actually being at codon 103 in the final coding region.

Barnase K27A

The barnase K27A mutation was selected based upon a report that the corresponding mutation in a related enzyme, binase, had approximately 20% of the activity of the native enzyme. Yakovlev et al. FEBS Lett. 354: 305-306 (1994). Another report suggests that barnase K27A mutant has reduced activity compared with native enzyme. Mossakowska et al. Biochemistry 28: 3843-3850 (1989). The barnase coding region was altered so that the codon for lysine 27 was substituted by an alanine codon. Simultaneous amplification and directed mutagenesis of the barnase segment was accomplished using PCR. Primers BAR5NCO (5′-TGACAACCATGGCACAGGTTATCAACACGTTTGAC-3′, SEQ ID NO: 31) and BARK27AR (5′-TGCTTCTGATGCTGTAATGTAATTATCAG-3′, SEQ ID NO: 36) were used to amplify the 5′ portion of the coding region and primers BARK27AF (5′-AATTACATTACAGCATCAGAAGCACAAG-3′, SEQ ID NO: 37) and BAR3SAC (5′-GAAGAAGAGCTCTTGACCGATCAGAGTTTGAAG-3′, SEQ ID NO: 35) were used to amplify the 3′ portion of the coding region from the barnase cassette of plasmid pMT416. After amplification, the fragments were purified away from the primers and PCR reagents, and then were combined. Approximately 100 ng of each fragment was combined with 1× Stratagene High Salt Buffer, 0.175 mM each dNTP and 0.25 μl TaqPlusLong in a 25 μl reaction, and the mixture was repeatedly denatured at 95° C., reannealed at 50° C. and incubated at 72° C. (five cycles) in order to allow extension of the complete coding region. The full barnase K27A fragment was further amplified by adding the extension reaction to a 75 μl mixture containing 20 μmol each of primers BAR5NCO and BAR3SAC, 1× Stratagene High Salt Buffer, 0.175 mM each dNTP and 0.75 μl TaqPlusLong, and running fifteen more cycles. The resulting full-length fragment was digested with NcoI and SacI and purified. The mutated coding sequence is set forth in SEQ ID NO: 8. As noted above, an extra Alanine codon was included immediately after the ATG in primer BAR5NCO. This resulted in the Lys to Ala mutation actually being at codon 28 in the final coding region.

Example 5 Assay for Toxicity of Barnase Mutants in E. coli

Barnase DNA was fused at the 3′ end of PrAG promoter by PCR, and the resulting PCR fragment was cloned into pUC19 and introduced into E. coli. After growing at 37 degrees C. overnight (16 hours) on LB agar supplied with 80 ug/ml ampicillin, single colonies were selected and inoculated into 1 ml of LB liquid containing ampicillin. After overnight incubation, the slow-growing E. coli cultures were selected and plasmids were extracted. The purified plasmids were reintroduced into E. coli, and single colonies were obtained on LB agar after overnight incubation at 37 degrees C. The diameters of the colonies were measured and compared with the control (pUC19 carrying the insert of barnase H102Y driven by PrAG promoter). The diameter of a single colony carrying a barnase mutant is the average of three independent experiments repeated from the step of introducing the plasmid into E. coli.

The toxicity of the barnase mutants was determined by comparing the diameter of the single colonies with control colonies. As shown below in Table 2, a large diameter colony indicates no toxicity, while a small diameter suggests strong toxicity.

TABLE 2 Toxicity of Barnase Mutants in E. coli Percentage of Colonies Number of Colony having Barnase Mutant Colonies on Diameter calculated Toxicity Construct Plate (mm) Diameter Level Control 245 0.8-1.0 85 None (*Barnase H102Y) Barnase H102E <300 0.9-1.1 85 None Barnase E73G 180 0.5-0.8 85 Medium Barnase F106S 320 0.2-0.5 95 High *Barnase H102Y has no biological RNase activity reported.

Example 6A Tissue-Preferred Expression of LPAG Promoter

Following the identification and cloning of a promoter by the procedure outlined above in Example 1, a promoter is operably linked with a reporter gene to determine those tissue types in which a promoter is active. To determine the tissue specificity of the LPAG1 and LPAG2 promoters, each promoter was operably linked to the GUS reporter gene and the resulting constructs were introduced into tobacco plants, as described in Example 2.

GUS Analysis of Sepals and Petals

Briefly, to analyze GUS expression of LPAG1 promoter activity in tobacco, sepals and petals were removed from unopened, young flowers that are about 2 to 5 mm in height. The carpels were cut vertically in the middle using a razor blade and the resulting half carpels (attached by 2-3 young stamens) were stained for GUS activity at 37° C. for 16 hours. Three individual flowers from each transgenic line were stained, and the destaining was carried out in 70% and then 95% ethanol.

GUS Analysis of Young Leaves

Young leaves adjacent to flowers were analyzed for GUS expression. For each transgenic line, three young leaves were cut into small squares (9 mm²) and stained for GUS activity at 37° C. for 16 hours, and then destained, as described above for the sepals and petals.

GUS Analysis of Vegetative Shoot Tips

Young shoot tips were collected from individual plants at two different stages of growth. Analysis of the first growth stage encompassed collecting shoot tips from tobacco plants in which 30% of the flowers on the primary terminal inflorescence were already open. This first growth stage analyzed the shoot tips with primary terminal inflorescences. The shoot tips with primary terminal inflorescences represent the axillary shoot tips growing out from the intersection of the primary stems and the primary leaves. Each shoot tip having a primary terminal inflorescence is about 10 to 15 mm long.

Analysis of the second growth stage encompasses collecting shoot tips 6 days post removal of the primary terminal inflorescence. These shoot tips do not have primary terminal inflorescence and represent the axillary shoot tips growing out from the intersection of the primary stems and the primary leaves. Each collected shoot tip without a primary terminal inflorescence is about 25 to 40 mm long.

Most of young leaves surrounding the shoot tips were removed and only one to three leaves were attached to the shoot tips. The dissected shoot tips were cut vertically in the middle and the resulting half tips (still attached by 1-3 leaves) were stained for GUS activity at 37° C. for 16 hours. Three shoot tips were collected and stained from each transgenic line.

As shown below in Table 3, LPAG1 promoter is preferentially active in the stamens and carpels (reproductive tissues) and shows no activity in leaves (vegetative tissues).

TABLE 3 GUS Expression Analysis of LPAG1 Activity in Transgenic Tobacco Analysis of Analysis of vegetative shoot vegetative shoot tips when tips when primary terminal primary terminal Stamens and Young inflorescence is inflorescence is Line No. Carpels Leaves present absent 1 NO NO Not tested Not tested 2 YES- NO YES-Medium NO Medium Expression Expression 4 YES- NO YES-Strong YES-Weak Strong Expression Expression Expression 5 YES- NO YES-Medium NO Medium Expression Expression 6 YES- NO YES-Medium NO Medium Expression Expression 7 YES- NO YES-Medium NO Medium Expression Expression 8 YES- NO YES-Medium NO Medium Expression Expression 9 YES- NO YES-Strong YES-Medium Strong Expression Expression Expression 11 YES-Weak NO NO NO Expression 12 YES- NO YES-Medium YES-Weak Medium Expression Expression Expression 13 YES- NO YES-Weak NO Medium Expression Expression 14 YES- NO YES-Strong YES-Medium Strong Expression Expression Expression 15 YES-Weak NO YES-Weak NO Expression Expression 16 YES- NO YES-Medium NO Strong Expression Expression 17 YES-Weak NO YES-Weak NO Expression Expression 18 YES-Weak NO YES-Weak NO Expression Expression

As shown above in Table 3, LPAG1 promoter activity decreases in shoot tips following removal of the primary terminal inflorescence. In the presence of the primary inflorescence, the vegetative growth of axillary buds is suppressed, and the transition from vegetative buds to reproductive buds is very fast. In some cases, the floral buds emerged when the axillary shoots are only 10 mm in length. During reproductive growth in tobacco, nutrient acquisition and hormone production induce floral gene expression in the axillary shoots. Removal of the primary terminal inflorescence resets the tobacco plants back to vegetative growth, and the growth of axillary buds is no longer subject to the suppression imposed by the terminal flowers.

It was observed that after the removal of the primary terminal inflorescence the axillary buds grow fast and the floral buds are not present when the axillary shoots are 40 mm long. So, in the presence of the terminal flowers, the meristems of axillary shoots are already converted to floral meristems or half way towards floral meristems in which the expression of floral genes, such as LEAFY and AGAMOUS, is turned on, and LPAG1 promoter is also turned on. The removal of the terminal flowers resets the axillary buds back to vegetative growth and the expression of floral genes in the axillary shoot meristems is turned off, and so LPAG1 promoter activity is probably also turned off.

Example 6B Deletion Analysis of LPAG1 Promoter

Promoter deletion analysis can be used to determine the minimal promoter and regulatory elements within a promoter sequence. Each promoter deletion is operably linked to a reporter gene and the expression profile of the promoter-reporter gene construct is analyzed.

For example, LPAG1 promoter (SEQ ID NO. 1) was serially deleted. Briefly, five serial deletions were made from the 5′-end of the LPAG1 promoter sequence. Each serial deletion deletes approximately 160 bp, for a total of a 800 bp deletion. The following is a summary of preliminary results of LPAG1 promoter deletion. The five serial deletion constructs (dentoted LPAG1d1-LPAG1d5) were introduced into pine and tobacco. Because the deletions are made from the 5′-end of the LPAG1 promoter sequence, it was estimated that the LPAG1d5 deletion construct should cut into the 5′ untranslated region of LPAG1 gene and therefore, the LPAG1 promoter sequence should be absent from the LPAG1d5 construct.

Following transformation of pine and tobacco plants with the promoter-deletion constructs, as described in Example 2, transformed calli were analyzed for LPAG1 promoter activity. GUS expression analysis was determined as outlined in Example 5. The results of the LPAG1 promoter deletion experiments are summarized below in Table 4.

TABLE 4 Promoter deletion analysis of LPAG1 Relative Activity Relative Activity in in Tobacco Construct Promoter Length Pine calli Flowers LPAG1 1400 Strong Strong LPAG1 d1 1240 Same as full-length Same as full-length promoter promoter LPAG1 d2 1080 Same as full-length Same as full-length promoter promoter LPAG1 d3 920 Same as full-length Same as full-length promoter promoter LPAG1 d4 760 Same as full-length Very low GUS promoter activity detected LPAG1 d5 600 NO GUS staining NO GUS staining activity detected activity detected

Based on the GUS expression profiles displayed in Table 4, the results clearly suggest that the nucleotide sequences (˜150 bp) which are present in LPAG1d3 but absent in LPAG1d4 are essential for the LPAG1 promoter to be active in the stamens and carpels of tobacco flowers, but the same sequences are not essential for the LPAG1 promoter to be active in pine calli since LPAG1d4 still have similar GUS activities in the calli as indicated by GUS staining and MUG assays.

Example 7 Method for Ablating Pine Male and Female Cones Using a Construct having LPAG1 and PrAG Promoters

Based on the results shown in Example 6, Table 4, the LPAG1 and PrAG promoters and its promoter deletions can be used for ablating male and female cones in Pine trees.

For example, an ablation construct could have the LPAG1 promoter operably linked to a gene encoding barnase, while the PrAG or LPAG1d4 promoter is operably linked to a gene encoding barstar (barnase inhibitor). As shown above in Example 6, LPAG1 promoter is active in pine cones and embryos while the PrAG or LPAGd4 promoter is active only in pine embryos. By placing the gene encoding barstar under a promoter (PrAG) that shows little activity in a pine cone, barnase toxicity produced by the other promoter (LPAG) can effectively ablate male and female cones. On the other hand, similar levels of activities of the two promoters in pine embryos produce similar amounts of barnase and barstar, and so the barnase toxicity in the embryos is effectively neutralized, leading to transformation and regeneration of pine embryogenic calli and enbryos. Following the transformation protocols described in Example 2, pine calli are analyzed for LPAG1 expression.

Example 8 Analysis of AGAMOUS Promoter from P. radiata

As described in Example 1, a reproductive-preferred promoter can be identified and cloned from a tree species, such as P. radiata or E. grandis. The PrAG promoter is an AGAMOUS promoter from P. radiata. The PrAG promoter has a length of about 1400 bp, including a 5′-untranslated region. The PrAG promoter is disclosed in WO 00/55172, which is incorporated herein by reference.

To determine whether PrAG confers reproductive-preferred expression, the PrAG promoter was operably linked to a GUS reporter gene having an intron. The resultant PrAG-GUS promoter construct was introduced into tobacco plants, as described in Example 2. Tobacco tissues were analyzed for GUS expression and Table 5 summarizes PrAG promoter activity.

TABLE 5 GUS analysis of PrAG promoter activity Tobacco Tissue Sample GUS Expression Level Leaf None Petal Yes Stamen Yes Carpel Yes

Although GUS expression in leaf, petal, stamen, and carpel tissue was not detectable by enzymatic assay, GUS expression in petal, stamen, and carpel tissue was detectable using a more sensitive method, such as RNase Protection Assay with poly(A⁺) RNA.

Example 9 Floral Specific Enhancer Increases PrAG Promoter Activity

As illustrated in Example 8, the PrAG promoter confers very weak reproductive-preferred promoter expression in tobacco. It has been shown that the Arabidopsis AGAMOUS gene contains a floral-specific enhancer (AtAGenh) that resides in the second intron of the A G gene. Sieburth, L. E., and Meyerowitz, E. M. The Plant Cell 9, 355-365 (1997). Busch, M. A., Bomblies, K., and Weigel, D. Science 285, 585-587 (1999). Deyholos, M. K., and Sieburth, L. E. The Plant Cell 12:1799-1810 (2000). It is possible that the AtAGenh enhancer element may upregulate PrAG promoter activity preferentially in the reproductive tissues of angiosperm flowers.

To determine whether AtAGenh enhances PrAG promoter activity in reproductive tissues, the second intron of Arabidopsis AG (2750 bp) was isolated and fused to the 5′ end of the PrAG promoter operably linked to the GUS reporter gene having an intron ((AtAGenh)PrAG::GUSIN), and the resulting construct (pWVCZ20, See FIG. 2) was introduced into tobacco.

Following tobacco transformation, tobacco tissues were collected and analyzed for GUS expression. As indicated in Table 6 below, GUS staining revealed that, indeed, the AtAGenh enhances PrAG promoter activity primarily in the stamen and carpel, and some increase was also observed in the petal. No GUS staining was observed in sepal, leaf, and the vegetative shoot tip.

TABLE 6 AtAGenh Enhances PrAG promoter Activity Tobacco Tissue GUS Expression GUS Expression Sample PrAG::GUSIN (AtAGenh)PrAG::GUSIN Stamen Weak Expression Enhanced GUS Expression Carpel Weak Expression Enhanced GUS Expression Petal Weak Expression Enhanced GUS Expression Sepal NO GUS NO GUS Expression Expression Leaf NO GUS NO GUS Expression Expression Vegetative Shoot NO GUS NO GUS Expression Expression

Example 10 Use of a Reproductive-Preferred Promoter::Mutant Barnase Construct for Reproductive Ablation without Disturbing Vegetative Growth

As described above in Example 4, various methodologies may be used to produce mutant cytotoxic genes having attenuated cytotoxic effects. By reducing the toxic effect of a barnase enzyme, barnase may be used for reproductive ablation, without compromising a plant's vegetative growth. Moreover, the combination of a reproductive-preferred promoter operably linked to an attenuated barnase provides a means for reproductive ablation, without vegetative destruction. For example, mutant barnase E73G was fused with PrAG to create pWVCZ23 (FIG. 3) and (AtAGenh)PrAG to create pWVCZ24 (FIG. 4), respectively, and the resulting constructs were introduced into tobacco. Following transformation, the tobacco plants were analyzed and the results are shown below in Table 7.

TABLE 7 Percentage of Percentage of total transgenic total transgenic plants plants Negative recovered that recovered that Effects on Flower do not produce do not produce Vegetative Transformation Construct Phenotype pollen. (%) seed. (%) Growth (AtAGenh)PrAG::E73G Degenerated 68 68 NO stamen and carpel; retarded petal; normal sepal PrAG::E73G Normal 10 10 NO

As shown in Table 7, 68% of tobacco plants transformed with (AtAGenh)PrAG::E73G have a sterile reproductive phenotype, i.e., many transformed plants produced neither viable pollen nor viable seeds. Likewise, 10% of plants transformed with PrAG::E73G produced no viable pollen and seeds. Interestingly, transformation with either construct does not compromise vegetative growth. The above results clearly demonstrate that the ablation cassette, (AtAGenh)PrAG::barnaseE73G, can produce male- and female-sterile tobacco, and this cassette may be able to produce similar ablation effects on other angiosperm plants, including angiosperm and gymnosperm species.

Example 11 Use of a Temperature-Sensitive Barnase for Ablating Reproductive Primordia without Disturbing Vegetative Growth

Barnase is a well-characterized enzyme, and numerous mutants have been identified. In particular, barnase mutants having altered stability and/or toxicity have been identified. A temperature-sensitive barnase may be desirable for ablating reproductive primordia without affecting vegetative growth.

For example, a heat-sensitive barnase could be used for reproductive ablation. Expression of a heat-sensitive barnase, for example, may have little toxic effect during the summer (high temperature) when the majority of vegetative growth occurs, but may be toxic during the winter or low temperature production of reproductive buds. A reproductive-preferred promoter, such as PrMC2 (SEQ ID NOs 4 or 16) could be used for minimizing expression of a heat-sensitive barnase in vegetative tissues.

Example 12 Barstar Neutralizes Barnase Toxicity in Transgenic Pine Calli and Regenerated Embryos

Barstar is a natural inhibitor of barnase, and it has been used for protecting non-targeted tissues from barnase toxicity and for restoring plant fertility. Beals T. P. and Goldberg R. B. Plant Cell. 9:9:1527-45 (1997). Kuvshinov V et al. Plant Sci. 160:3:517-522 (2001). Previous experiments demonstrate that three promoters, LPAG1, PrAG, and LPAG1d4, have similar activities in pine calli and regenerated embryos. While LPAG1 promoter has high activity in tobacco flowers, the PrAG and LPAG1d4 promoters showed no or trace activities in the tobacco flowers, suggesting that PrAG and LPAG1d4 promoters may not be active in angiosperm or gymnosperm reproductive tissues. Thus, the PrAG and LPAG1d4 promoters could be operably linked to a gene that neutralizes the cytotoxic effects of barnase, such as barstar, and the promoter::barstar construct would target non-reproductive tissues. Such a promoter::barstar construct, for example PrAG::barstar, would protect vegetative tissues from deleterious barnase expression.

Moreover, it may be beneficial to create an ablation construct having a reproductive-preferred promoter operably linked to barnase and a non-reproductive-preferred promoter operably linked to barstar. For example, a pine cone ablation construct could have the LPAG1 promoter driving barnase while the PrAG or LPAG1d4 promoter drives barstar (such as LPAG1::barnase E73G/PrAG::barstar or LPAG1::barnase E73G/LPAG1d4::barstar), with both cassettes in one backbone. During pine transformation, the toxicity of barnase due to LPAG1 activity in pine calli and regenerated embryos will be effectively neutralized by the barstar produced by the activity of PrAG or LPAG1d4 promoter, and thus the transformation can proceed smoothly. However, in the mature transgenic pine trees, the presence of barnase in the pine-cone buds, due to LPAG1 promoter activity, will effectively kill the cones because of barnase toxicity and the lack of the barstar in the pine-cone buds.

Example 13 Cloning of In-Frame PrMC2.400 Promoter Fragments

The PrMC2.400 promoter sequence was identified and isolated at described in U.S. Patent Application Publication 20030101487, which is incorporated by reference. The PrMC2.400 sequence has an ATG that is not in-frame with the ATG used in pWVR220 and other PrMC2 constructs. Although previous tests in Arabidopsis clearly showed that GUS is expressed from the PrMC2.400 promoter, GUS expression has not been observed in anthers of tobacco transformed with the PrMC2.400 promoter. Accordingly, an in-frame PrMC2.400 promoter was cloned for use in an ablation construct.

Using the PCR primers below, two different PrMC2.400 promoter sequences were isolated. As described below, the two PrMC2.400 promoters were cloned into expression vectors to ensure that the sequences are in-frame with an operably linked gene.

There are several in-frame ATGs in the PrMC2.400 promoter sequence, particularly at positions 361, 367, and 397. Using the reverse primers described, two different PrMC2.400 products were produced: PrMC2.400-1 contains all three ATGs; PrMC2.400-3 contains only the first ATG. The reverse primers were phoshorylated at the 5′ end so they could be blunt-ligated to the appropriate sites in a cloning vector. The PrMC2-XG primer contains an XhoI site. PCR was performed using a high fidelity Taq polymerase blend (TaqPlus Long, Stratagene). After PCR, the amplification products were gel purified and then digested with XhoI using standard procedures. Each product was cloned into an intermediate vector and sequenced. Sequencing indicated that the PrMC2.400-1 sequence differed by one nucleotide from the original sequence, there is an insertion of a ‘T’ residue at position 35.

The cloning of the PrMC2.400-1 and PrMC2.400-3 sequences into expression vectors has ensured that all ATG sites remain in-frame with a gene of interest.

PrMC2-XG (for): (SEQ ID NO: 38) 5′-GAAGAACTCGAGTAAAACATAATTTTGGCAGTAAAAAGTGA-3′ PrMC2-R1 (rev): (SEQ ID NO: 39) 5′-CATGTTCCCGTTTGATACCTGAATTTTG-3′ PrMC2-R3 (rev): 5′-CATAAATCTTCTAAAAACAGCAGAACTGAC-3′

(SEQ ID NO: 40)PrMC2-XG+PrMC2—R1: produced a 3966(KNC) bp product designated PrMC2.400-1 (SEQ ID NO: 5)

PrMC2-XG+PrMC2—R3: produced a 3603(KNC) bp product designated PrMC2.400-3 (SEQ ID NO: 16)

Example 14 Cloning In-Frame PrMC2.400-1::Mutant Barnase into Binary Vectors

As described in Example 17, the in-frame promoters PrMC2.400-1 and PrMC2.400-3 may be operably linked to a gene of interest for genetic ablation. For example, the in-frame PrMC2.400-1 promoter may be operably linked to an attenuated barnase sequence for reproductive ablation.

K27A

As described in Example 4, the K27A mutant barnase was previously cloned into a high copy vector, pWVR63. The PCR generated fragment PrMC2.400-1 was cloned into pWVR63 previously digested with NcoI, Mung bean nuclease treated to generate a blunt-end, followed by an XhoI digest and gel purification to isolate the vector fragment. The subsequent intermediate plasmid, pWVR205, now contained the ablation cassette PrMC2.400-1::K27Abarnase::RNS2TER. This cassette was then subcloned into a binary vector using KpnI and ApaI to generate pWVR216.

H102E

As indicated in Example 4, the H102E mutant barnase was previously cloned into a high copy vector, pWVR15. In order to have more convenient restriction enzyme ends for cloning, H102E was generated using PCR primers from pWVR15 template. The mutant barnase H102E was generated using PCR primers:

Agl2-PB: (SEQ ID NO: 33) 5′-TTTCACAACCTCCACACACTT-3′ Bar3Sac: (SEQ ID NO: 35) 5′-GAAGAAGAGCTCTTGACCGATCAGAGTTTGAAG-3′

PCR was performed using a high fidelity Taq polymerase blend (TaqPlus Long, Strategene). Standard three-step PCR methodology was used. The PCR reaction was gel purified and subsequently digested with NcoI and SacI. The restriction digest was gel purified and the fragment isolated and concentrated. This purified PCR fragment was cloned into an intermediate vector previously digested with NcoI and SacI, producing the construct pWVR218. This construct was sequenced to ensure correct mutant barnase sequence. The PCR generated fragment PrMC2.400-1 was then cloned into pWVR218 previously digested with NcoI, Mung bean nuclease treated to generate a blunt-end, followed by an XhoI digest and gel purification to isolate the vector fragment. The subsequent plasmid, pWVR219, now contained the ablation cassette PrMC2.400-1::H102Ebarnase::RNS2TER. This construct was sequenced to ensure correct promoter sequence and promoter:gene junction. This cassette was then subcloned into a binary vector using KpnI and ApaI to generate pWVR220.

E73G

E73G mutant barnase was previously cloned into a high copy vector, as indicated in Example 4. In order to have more convenient restriction enzyme ends for cloning, E73G sequence was generated using PCR primers from a plasmid template. The mutant barnase E73G was generated using PCR primers:

Bar5Nco: (SEQ ID NO: 31) 5′-TGACAACCATGGCACAGGTTATCAACACGTTTGAC-3′ Bar3Sac: (SEQ ID NO: 35) 5′-GAAGAAGAGCTCTTGACCGATCAGAGTTTGAAG-3′

PCR was performed using a high fidelity Taq polymerase blend (TaqPlus Long, Strategene). Standard three-step PCR methodology was used. The PCR reaction was gel purified and subsequently digested with NcoI and SacI. The restriction digest was gel purified and the fragment isolated and concentrated. This purified PCR fragment was cloned into an intermediate vector previously digested with NcoI and SacI producing the construct pWVR230. This construct was sequenced to ensure correct mutant barnase sequence. The PCR generated fragment PrMC2.400-1 was then cloned into pWVR230, previously digested with NcoI, Mung bean nuclease treated to generate a blunt-end, followed by an XhoI digest and gel purification to isolate the vector fragment. The subsequent plasmid, pWVR231, now contained the ablation cassette PrMC2.400-1::E73 Gbarnase::RNS2TER. This construct was sequenced to ensure correct promoter sequence and promoter:gene junction. This cassette was then subcloned into a binary vector using KpnI and ApaI to generate pAGF232.

GUS Control

Although previous tests in Arabidopsis demonstrated that GUS is expressed from the original PrMC2.400 promoter, no staining has been observed in transformed tobacco anthers. A new reporter cassette (see below) was synthesized so that it matches the frame of the ablation constructs.

The PCR generated fragment PrMC2.400-1 was cloned into pWVR52, previously digested with NcoI, Mung bean nuclease treated to generate a blunt-end, followed by an XhoI digest and gel purification to isolate the vector fragment. The subsequent plasmid, pWVR233, now contained the cassette PrMC2.400-1::GUS::RNS2TER. This construct was sequenced to ensure correct promoter sequence and promoter:gene junction. This cassette was then subcloned into a binary vector using KpnI and ApaI to generate pAGF234.

Example 15 In Planta Expression of PrMC2.400-1: Barnase

Agrobacterium tumefaciens strain GV2260 was transformed via electroporation with binary vector pWVR216 or pWVR220 or pAGF232 or pAGF234.

Transgenic plants were produced by Agrobacterium-mediated transformation of tobacco (Nicotiana tabacum). Transformants were selected on a medium containing kanamycin. Positive transformants were identified by PCR, transferred to soil, and grown under standard greenhouse conditions. Plants were analyzed for overall vegetative growth rate, time of flowering and male-sterility.

Plants expressing the mutant barnase genes driven by the PrMC2.400-1 promoter displayed a male-sterile phenotype. Specifically, the transgenic plants did not produce pollen grains. This was confirmed microscopically, by observing anthers under a compound light microscope. Further, the pollenless plants did not produce fruit capsules and seeds. However, when the plants were cross-pollinated with wt tobacco pollen, normal seed set occurred, indicating that female fertility was unaffected. Additionally, offspring from these cross-pollinations produced a pollenless phenotype, indicating that the transgenes were inherited and the presence of the transgene in the progeny produced male sterile plants.

It was noted that tobacco lines expressing the mutant barnase gene driven by the PrMC2.400-1 promoter had a reduced stamen height, relative to the carpel. Flowering time was also delayed. A reduction in vegetative growth was readily observed for tobacco lines expressing K27A and E73G, relative to the control lines. This reduction in vegetative growth resulted in shorter plants with slower development. Lines expressing H102E showed minimal signs of vegetative effects and were very similar to controls in overall growth. The reduction in vegetative growth could be an indication of ‘leakiness’ of the expression of the PrMC2.400 promoter in tobacco tissue.

To assay PrMC2.400 promoter activity in vegetative tissues, young leaf tissue, roots, and vegetative shoot tips from lines transformed with PrMC2.400-1::GUS lines were tested for GUS activity. GUS activity was assayed histochemically using the chromogenic substrate X-Gluc. Tissues were vacuum-infiltrated in X-Gluc at room temperature for 1 hour then incubated at 37° C. for 16 hours. Following incubation, the tissues were destained in 100% methanol and then 95% ethanol. These tissues displayed no GUS expression. It is possible that the level of GUS expression is so low that it cannot be detected by this assay.

Additional experiments using PrMC2.400-1 linked to GUS were performed to further understand temporal and spatial expression patterns during anther development in tobacco. Tobacco flower development can be divided into 12 stages to provide reference points for the expression of genes in floral organ systems. Koltunow, et al. The Plant Cell 2:1201-1224 (1990). Flower buds were removed at each stage, dissected, stained for GUS activity, and observed microscopically. GUS activity was assayed histochemically using the chromogenic substrate X-Gluc. Floral buds were vacuum-infiltrated in X-Gluc at room temperature for 1 hour then incubated at 37° C. for 16 hours. Tissue was destained in 100% methanol and then 95% ethanol. The results indicate that the PrMC2.400-1 promoter is expressed in only in the anther, and PrMC2.400-1 expression is limited to those developmental stages in which the tapetum is present. The tapetum layer plays a major role in pollen formation. Therefore, expression of a cytotoxic gene in the tapetum layer could prevent pollen production.

Example 16 Cloning PrMC2.400-3::Mutant Barnase into Binary Vectors

H102E

PrMC2.400-3 was generated using primers PrMC2-XG and PrMC2-R3, as described above in Example 13. Template used to amplify this fragment was the binary vector, pWVR220. This purified PCR fragment was cloned into an intermediate vector previously digested with NcoI and SacI, producing the construct pWVR242, which now contained the ablation cassette PrMC2.400-3::H102Ebarnase::RNS2TER. This construct was sequenced to ensure correct promoter sequence and promoter:gene junction. This cassette was then subcloned into a binary vector using KpnI and ApaI to generate pWVR243.

GUS Control

The PCR generated fragment PrMC2.400-3 was cloned into pWVR52 previously digested with NcoI, Mung bean nuclease treated to generate a blunt-end, followed by an XhoI digest and gel purification to isolate the vector fragment. The subsequent plasmid, pWVR244, now contained the cassette PrMC2.400-3::GUS::RNS2TER. This construct was sequenced to ensure correct promoter sequence and promoter:gene junction. This cassette was then subcloned into a binary vector using KpnI and ApaI to generate pWVR245.

Example 17 In Planta Expression of PrMC2.400-3: Barnase

Agrobacterium tumefaciens strain GV2260 was transformed via electroporation with binary vector pAGF243 or pAGF245.

Transgenic plants were produced by Agrobacterium-mediated transformation of tobacco (Nicotiana tabacum). Transformants were selected on a medium containing kanamycin. Positive transformants were identified by PCR, transferred to soil, and grown under standard greenhouse conditions. Plants were observed for overall vegetative growth rate, time of flowering and male-sterility. Transgenic tobacco lines displayed a male-sterile phenotype. Specifically, the plants did not produce pollen grains. Additonally, the PrMC2.400-1::H102E lines had reduced stamen height, relative to carpel height, and flowering time was delayed.

Lines containing PrMC2.400-3 linked to the reporter gene GUS were compared with PrMC2.400-1::GUS lines. The intensity of GUS staining in floral buds, specifically anther tissue, was comparable to the PrMC2.400-1::GUS lines.

Example 18 Construction of Precursor Plasmids with Flowering Control Cassettes

Construction of the plasmids began with a binary vector derived from pBIN19 that was reduced in size through deletion of nonessential DNA segments, pARB310 (SEQ ID NO: Z1). A gene for barstar (Hartley, R. W. J. Mol. Biol. 202: 913-915 (1988)) that had been previously cloned with flanking BstXI sites was removed from pWVR200B by BstXI digestion and gel purified. The approximately 470 bp fragment was ligated into pARB310 that had been digested with BstXI, to produce pARB310B.

Next, the ColE1 replication origin and surrounding region were amplified from pART27 (Gleave, 1992) using PCR with the primer pair, ColE1-F4 (5′-GAGAGAGGATCCGGTGTGAAATACCGCACAG-3′, SEQ ID NO: 41) and ColEL1-R4 (5′-GAGAGATGATCAGCCTCACTGATTAAGCATTGGTAACTG-3′, SEQ ID NO: 42). The 1.0 kb ColE1 fragment was digested with BamHI and BclI, then was purified and ligated into the BclI site of pARB310B, between the end of the trfA gene and the left border (LB) of the T-DNA. This generated pAGF50, which acted as a high copy number plasmid in E. coli, but still replicated in Agrobacterium.

pAGF50 was digested with AscI and NcoI to remove the UBQ3 promoter plus most of the NPTII coding region, and the resulting 5.7 kb fragment was gel purified. The 1.9 kb fragment with UBQ10 promoter linked to the 5′-end of the NPTII coding region was released from pWVR3 by AscI and NcoI digestion, gel purified, and ligated into the pAGF50 fragment to generate pARB1000. This plasmid was further modified by the addition of a SUBIN::GUSIN::NOSTER reporter cassette. SUBIN indicates a ubiquitin promoter from P. radiata, which included genomic DNA coding the 5′-UTR and an intron; GUSIN indicates the β-glucuronidase coding region plus an intron from the potato tuberin gene (Vancanneyt et al., 1990). The reporter cassette was removed from pARB494 by DraI digestion and ligated into the SmaI site of pARB1000 to generate pARB1001. In addition to being able to serve as a transformation control, pARB1001 was used as the direct precursor to the flowering control plasmids because it had two NotI sites flanking the reporter gene, which could be used to switch it with other genes of interest.

The male-specific flowering control gene, PrMC2.400::barnaseH102E::RNS2TER, was present in pWVR219, with an unwanted NotI site near the 3′-end. The plasmid was digested with NotI, and then the site was destroyed by treating with T4 DNA polymerase in the presence of dNTPs and religating the vector. The PrMC2.400::barnaseH102E::RNS2TER cassette was excised from the altered pWVR219 with AscI and XhoI, and the 1.1 kb fragment was gel purified. pARB1001 was prepared by partial digestion with XhoI to linearize the plasmid, followed by complete digestion with AscI. The PrMC2.400::barnaseH102E::RNS2TER cassette was ligated to the prepared pARB1001 vector to generate pARB1002. The structure of the plasmid was verified with single-pass sequencing.

The (AtAGenh)PrAG::barnaseE73G::NOSTER cassette was removed from pWVCZ24 by EcoRI and AscI digestion. A NotI adapter comprising the oligonucleotides, EcoNot1 (5′-AATGCGGCCGCAGAGA-3′, SEQ ID NO: 43) and EcoNot2 (5′-TCTCTGCGGCCGC-3′, SEQ ID NO: 44), was ligated to the EcoRI site and digested with NotI, and then the 4.9 kb fragment was purified. The plasmid pARB1001 was digested with NotI and AscI and the 7.6 kb vector fragment was gel purified. The above cassette was ligated into these sites to generate pARB1005L (FIG. 19, SEQ ID NO: 27). The structure of the plasmid was verified with single-pass sequencing.

Example 19 Transformation of Early Flowering Eucalyptus occidentalis

This example details the infection and transformation of early flowering Eucalyptus occidentalis. In order to test flowering control constructs. Eucalyptus occidentalis seedlings were tested for early flowering in glasshouse growing conditions, and clones were selected on the basis of flowering within six months. These clones were introduced into sterile tissue culture for transformation with ablation constructs of the instant invention and control GUS constructs. Leaf explants were harvested and pre-cultured for 4 days and then separate explants were infected with Agrobacterium strain GV2260 harboring p35SGUSINT (35S:: GUSINT, NOS::NPTII) or the constructs of the instant invention, as shown in the table below, according to the method of U.S. patent application Ser. No. 10/861,909, which is incorporated herein by reference. Following eradication of the Agrobacterium, explants were transplanted to selection medium, which consisted of regular regeneration medium as described in that same patent application, with 30 mg/l Geneticin. Regenerated shoots of the transformants and were rooted and grown in containers on soil in a glasshouse for testing the Eucalyptus transformed with ablation constructs for flowering time relative to controls.

Constructs of the instant invention were also transformed into clones of Eucalyptus camaldulensis and commercial clones of Eucalyptus urophylla and Eucalyptus grandis using the method of U.S. patent application Ser. No. 10/861,909. Regenerated shoots of the transformants were rooted, transferred to soil and acclimated in a glasshouse, then transferred to field planting sites in Florida and South Carolina under notifications to the US Agricultural Plant Health Inspection Service. Plants are monitored regularly for the development of floral buds. No flowering has been observed to date.

TABLE 8 Any effects noted in tissue culture Attenuated suggesting leakiness Barnase Approx date into of the promoter Flowering Gene (for transformation driving the Name of Control example, Euc species and (or planned to attenuated barnase Construct Promoter H102E) clone transform) gene pARB598 PrMC2 H102E E. occidentalis December 2003 None clones 129 and 208 pAGF243 PrMC2.400-3 H102E E. occidentalis clone March 2004 129 pARB598 PrMC2 H102E E. urophylla clone June 2003 None IPB1 pARB599 PrMC2 H102E E. urophylla clone June 2003 Reduced IPB1 transformation efficiency relative to control pARB675 PrMC2 H102E E. urophylla clone April 2004 IPB1 pARB639 PrAG E73G E. urophylla clone June 2003 Could not recover IPB1 lines with all T-DNA components. pWVCZ24 PrAG E73G E. camaldulensis March 2003 None clone C9 pWVCZ101 PrAG E73G E. camaldulensis March 2003 None clone C10 pWVCZ24 PrAG E73G E. grandis clone IP1 April 2003 None pWVCZ101 PrAG E73G E. grandis clone IP1 April 2003 None pWVR220 PrMC2 H102E E. grandis clone IP1 April 2003 None pAGF232 PrMC2 E73G E. grandis clone IP1 April 2003 None

Example 20 Hybrid pine

Hybrid pine (P. taeda×P. rigida) and loblolly pine (P. taeda) embryogenic cell lines were initiated from zygotic embryos of individual immature megagametophytes using the procedures described in U.S. Pat. No. 5,856,191, and maintained using the procedures described in U.S. Pat. No. 5,506,136.

After one to three months of culture on maintenance medium, the tissue cultures were cryopreserved, stored for periods of up to several years, and then retrieved using the methods of U.S. Pat. No. 6,682,931. Those skilled in the art of plant tissue culture will recognize that other cryopreservation and recovery protocols would be applicable to the present method and that the detail in this example may not be construed to limit the application of the method.

Uniform suspension cultures from two genetically different hybrid pine tissue culture lines and multiple P. taeda lines were established by inoculating a 250 ml Nephelo sidearm flask (Kontes Chemistry and Life Sciences Products) with 1 g of tissue each according to the method of U.S. Pat. No. 5,491,090. The flasks containing the cells in liquid medium were placed on a gyrotory shaker at 100 rpm in a dark culture room at a temperature of 23° C.±2° C. One week later, the liquid in each flask was brought to 35 ml by pouring 15 ml fresh medium into the culture flask and swirling to evenly distribute the cells. Cell growth was measured in the sidearm by decanting cells and medium into the sidearm portion of the flasks, allowing the cells to settle for 30 minutes and then measuring the settled cell volume (SCV). When the SCV was greater than or equal to half the maximal SCV (50% of the volume of the flask was occupied by plant cells), each culture was transferred to a 500 ml sidearm flask containing a total of 80 ml cells and medium and the transferred culture was maintained under the same conditions.

To prepare for gene transfer, polyester membrane supports were sterilized by autoclaving and placed in separate sterile Buchner funnels, and for each of six replicate plates per cell line, one to three milliliters of pine embryogenic suspension was pipetted onto each support such that the embryogenic tissue was evenly distributed. The liquid medium was suctioned from the tissues and each support bearing the embryogenic tissue was placed on gelled preparation medium for Agrobacterium inoculation according to the methods described in U.S. Patent Publication No. 20020100083. Binary reporter gene constructs were introduced into different isolates Agrobacterium tumefaciens by techniques well known to those skilled in the art, and virulence was induced with administration of acetosyringone by commonly used techniques whereupon each of the induced Agrobacterium isolates was co-mingled with separate replicates of the plant material. The cells were co-cultivated in the dark at 22°±2° C. for approximately 72 hours.

Following co-cultivation, Agrobacterium was eradicated from the cultures according to the methods described in U.S. Patent Publication No. 20020100083. Cells borne on polyester membrane supports were then transferred onto fresh selection media at intervals of 2 weeks. Active growth on the selection medium occurred in a number of isolated sectors on many of the petri dishes. Such active growth in the presence of selection agent is normally an indication that the growing tissues have integrated the selection gene into their chromosomes and are stably transformed. These areas of active growth are treated as independent transformation events and are henceforth referred to as putative transgenic sublines. The putatively transgenic embryogenic tissue was multiplied by transferring growing transgenic sectors to fresh semi-solid maintenance medium supplemented with the respective selection agent.

Putatively transformed sublines, after reaching approximately 2 g, were chosen for polymerase chain reaction (PCR) amplification for verification of the presence of transgenes using standard techniques.

TABLE 9 Primer Pairs for PCR Product size virD2 GAA GAA AGC CGA AAT AAA GAG G 560 (SEQ ID NO: 45) virD2 TTG AAC GTA TAG TCG CCG ATA G (SEQ ID NO: 46) These primers were used to check contamination by Agrobacterium NptII AAG GAG ATA TAA CAA TGA TTG AAC 800 AAG ATG GAT TGC (SEQ ID NO. 47) NptII TCA GAA GAA CTC GTC AAG AAG G 800 (SEQ ID NO: 48) uid(gus) CGA AAA CGG CAA GAA AAA GCA G 450 (SEQ ID NO: 49) uid(gus) ACG ACC AAA GCC AGT AAA GTA G (SEQ ID NO: 50) Pal AAT GGG AAG CCT GAG TTT ACA 700 (SEQ ID NO: 51) Pal GGC CAG CAT GTT TTC CTC CAG (SEQ ID NO: 52) These primers, for the PAL gene, were used as a positive control

Material from each subline also was sacrificed for GUS staining and microscopic examination. For GUS staining, an inserted uidA gene, encoding a β-glucuronidase enzyme expressing in tissue culture cells, was detected by deep blue staining of cells from each of the transgenic lines upon exposure to a colorigenic glucuronidase enzyme substrate, “X-gluc,” commercially available from Inalco, according to techniques well known in the art of plant transformation. Microscopic examination demonstrates that cell division has resumed and that transient expression of the uidA transgene displays the normal frequency for these bombardments.

Germinable embryos were produced as follows. After the cell masses that had been cultured on selection medium proliferated to at least one gram, each was separately resuspended in liquid medium again. When the cell suspensions were brought to uniform (half-maximal) SCV, equivalent amounts of suspension culture cells were pipetted onto sterile membrane supports for placement on development/maturation medium as described in U.S. Pat. No. 5,506,136 to develop high quality harvestable stage 3 (cotyledonary) embryos. Dishes were incubated in a dark growth chamber at 23±2° C. The membrane supports were transferred to new petri dishes containing fresh medium every 3 weeks. At week 9, stage 3 (cotyledonary) embryos were visually analyzed for germination quality and harvested onto fabric supports on medium as described in U.S. Pat. No. 5,506,136, and incubated for about four weeks in the dark at a temperature of 4° C.±2° C. Next, embryos on their fabric supports were incubated above water in sealed containers for about three weeks in the dark at a temperature of 25° C.±2° C. Following the above two treatments, embryos on their fabric supports were transferred to medium germination medium and incubated for about three days in the dark at a temperature of 25° C.±2° C. Embryos were then removed from their fabric supports and placed onto the surface of fresh germination medium. Germination was conducted in the light at a temperature of 25° C.±2° C. Germination plates were examined weekly, over a period of about four weeks, and germinating embryos were transferred to MAGENTA® boxes containing 100 ml of germination medium for conversion to plantlets. MAGENTA® boxes containing developing plantlets were incubated in the light at 25° C.±2° C. for about eight to twelve weeks.

When the plantlets formed epicotyls (newly formed shoots of approximately two to four cm), they were transferred to containers filled with a potting mix [2:1:2 peat:perlite:vermiculite, containing 602 g/m³ OSMOCOTE fertilizer (18-6-12), 340 g/m³ dolomitic lime and 78 g/m³ MICRO-MAX micronutrient mixture (Sierra Chemical Co.)]. The plantlets were grown in a shaded greenhouse and misted infrequently for a period of about two weeks. They were removed from mist for acclimatization in the greenhouse for about four weeks. Plantlets were then transferred to outdoor shade for about six weeks for final acclimatization before moving to full-sun conditions. They were then grown in containers until conditions were ready for field planting.

Plants regenerated from loblolly pine (P. taeda) lines were also planted into the same field sites and no strobilus production has been observed in the field sites as long as six years after planting. However, unexpectedly, the transgenic hybrid pine lines produced strobili three years after planting. At that point the hybrid trees were approximately one meter in height, much smaller than the adjacent transgenic loblolly pine trees.

Table 10 below shows the results of a second planting that included the non-transgenic hybrid pine origin line as a control from somatic embryogenesis, a variety of seedling genotypes with the same parents that present a control that did not pass through tissue culture, and a total of 24 different transgenic lines generated from the 97LP0006 somatic embryogenic line using two different vectors, some transformed using biolistics and some using Agrobacterium, with multiple replicates of most lines for a total of over 250 plants, produced some strobili two years after planting and significant numbers of strobili within three years after planting. Tests were terminated following these observations.

TABLE 10 % trees showing #trees in Both % trees % trees both planting male % trees showing showing male and Reporter Transformation Transgenic from this No Female Male and showing female male female construct method line number line strobili strobili strobili female no strobili strobili strobili strobili Act2::GUS Agrobacterium 28 9 6 3 1 1 67%   33% 11% 11% Act2::GUS Agrobacterium 29 10 9 1 1 1 90%   10% 10% 10% Act2::GUS Agrobacterium 31 8 0 7 2 1 0%  88% 25% 13% Act2::GUS Agrobacterium 32 10 0 10 2 2 0% 100% 20% 20% Act2::GUS Agrobacterium 34 10 2 8 1 1 0%  80% 10% 10% Act2::GUS Agrobacterium 36 10 0 10 2 2 0% 100% 20% 20% Act2::GUS Agrobacterium 38 10 0 10 3 3 0% 100% 30% 30% Act2::GUS Agrobacterium 39 3 3 0 0 0 100%   0%  0%  0% Act2::GUS Agrobacterium 53 9 1 8 3 3 11%   89% 33% 33% Act2::GUS Biolistics 64 8 1 5 4 2 20%  100% 80% 40% UBQ3::GUS Agrobacterium 117 9 1 8 3 3 11%   89% 33% 33% UBQ3::GUS Agrobacterium 118 9 0 9 2 2 0% 100% 22% 22% UBQ3::GUS Agrobacterium 119 10 1 9 5 5 10%   90% 50% 50% UBQ3::GUS Agrobacterium 120 10 0 10 0 0 0% 100%  0%  0% UBQ3::GUS Agrobacterium 122 8 0 8 0 0 0% 100%  0%  0% UBQ3::GUS Agrobacterium 125 10 0 10 2 2 0% 100% 20% 20% UBQ3::GUS Agrobacterium 127 10 0 10 3 3 0% 100% 30% 30% UBQ3::GUS Agrobacterium 128 10 1 9 2 2 10%   90% 20% 20% n.a. Non-transgenic 97LP0006 7 2 5 0 0 29%   71%  0%  0% somatic embryogenesis control n.a. Non-transgenic pitch x 46 27 15 7 3 59%   33% 15%  7% zygotic plant loblolly control seedlings

The results shown in table 10 suggest that passage through tissue culture and transformation is necessary to achieving the inventive early strobili production result, as the SE control did not produce strobili, and few of the non tissue-cultured genotypes did. However, nearly all of the transgenics produced either male or female strobili or both at very high frequency. Only one of 18 transgenic lines did not produce strobili within three years. The result was independent of the transformation used and independent of the transformation vector used. This suggests that best mode is to use transgenic controls, e.g. transformed with reporter gene constructs, for comparisons intended to show the efficacy of reproduction control constructs such as the inventive ablation constructs.

The trees were, at the time the strobili were produced, approximately 1.2 meters average height, easily harvestable by a person of average height without specialised equipment.

This system was then used to test the reproduction control constructs of the instant application for their utility in gymnosperms, a test that would otherwise be impossible to carry out. The embryogenic callus provides an opportunity to test whether or not the promoters being tested are leaky in a gymnosperm and whether the attenuated barnase genes are detrimental when expressed in a leaky fashion (see column 4 in the table). Once the trees are regenerated and planted in the field, effects on date of strobilus formation relative to GUS-transformed controls can be measured within three years, upon which time the field test can be terminated. This will further allow for a faster rotation of expensive production forestry land for these field tests.

TABLE 11 What effects Plants to Approx date into Name of noted in field pine SE lines Construct Promoter Gene pine callus planting transformation transformed pWVR216 PrMC2.400 barnaseK27A None No Jul. 1, 2002 92AA0033 pWVR217 PrMC2.400 LPRNase1 None No Jul. 1, 2002 92AA0033 pAGF234 PrMC2.400-1 GUS NA Yes Dec. 6, 2002 97LP0033 pWVR220 PrMC2.400-1 barnaseH102E None Yes Dec. 6, 2002 97LP0033 pWVR216 PrMC2.400-1 barnaseK27A detrimental No Dec. 6, 2002 97LP0033 pAGF232 PrMC2.400-1 barnaseE73G detrimental No Dec. 6, 2002 97LP0033 pAGF245 PrMC2.400-3 GUS NA No Dec. 2, 2003 97LP0033 pAGF243 PrMC2.400-3 barnaseH102E None Yes Dec. 2, 2003 97LP0033

Example 21 Method for Ablating Pine Male and Female Cones Using a Construct Having LPAG1 and LPAG1d4 Promoters

Based on the results shown in Example 6, Table 4, the LPAG1 and LPAG1d4 promoters can be used for ablating male and female cones of pine trees. For example, an ablation construct could have the LPAG1 promoter operably linked to a gene encoding barnase, while the LPAG1d4 promoter is operably linked to a gene encoding barstar (barnase inhibitor). As shown above in Example 6, LPAG1 promoter is active in pine cones and embryos while the LPAG1d4 promoter is active only in pine embryos. This assumption is made based on the observation that LPAG1 has high activities in tobacco flowers while LPAG1d4 has little activities in tobacco flowers. By placing the gene encoding barstar under the control of LPAG1d4 promoter that may have little activity in a pine cone, barnase toxicity produced by the other promoter (LPAG1) can effectively ablate male and female cones. On the other hand, similar levels of activities of the two promoters in pine embryos produce similar amounts of barnase and barstar, and so the barnase toxicity in the embryos is effectively neutralized, leading to transformation and regeneration of pine embryogenic calli and embryos.

Description of Sequence Identifiers:

-   -   SEQ ID NO. 1—LPAG1     -   SEQ ID NO. 2—LPAG2     -   SEQ ID NO. 3—PrAG-ATenh     -   SEQ ID NO. 4—PrMC2.400-1     -   SEQ ID NO. 5—barnase mutant E73G (DNA)     -   SEQ ID NO. 6—barnase mutant F106S (DNA)     -   SEQ ID NO. 7—barnase mutant H102E (DNA)     -   SEQ ID NO. 8—barnase mutant K27A (DNA)     -   SEQ ID NO. 9—barnase mutant E73G (AA)     -   SEQ ID NO. 10—barnase mutant F106S (AA)     -   SEQ ID NO. 11—barnase mutant H102E (AA)     -   SEQ ID NO. 12—barnase mutant K27A (AA)     -   SEQ ID NO. 13—PrMC2+barnase mutant H102E     -   SEQ ID NO. 14—PrMC2+barnase mutant K27A     -   SEQ ID NO. 15—PrMC2+barnase mutant E73G     -   SEQ ID NO. 16—PrMC2.400-3     -   SEQ ID NO. 17—LPAG1d4     -   SEQ ID NO. 18—pWVR220 [PrMC2.400::barnaseH102E] (FIG. 1)     -   SEQ ID NO. 19—pWVCZ20 [(AtAGenh)PrAG::GUS(intron)] (FIG. 2)     -   SEQ ID NO. 20—pWVCZ23 [PrAG::barnaseE73G] (FIG. 3)     -   SEQ ID NO. 21—pWVCZ24 [(AtAGenh)PrAG::barnaseE73G] (FIG. 4)     -   SEQ ID NO. 22—pARB599B [PrMC2::barnaseH102E] (FIG. 5)     -   SEQ ID NO. 23—pARB639B [(AtAGenh)PrAG::barnaseE73G] (FIG. 6)     -   SEQ ID NO. 24—pAGF243 [PrMC2.400-3::barnaseH102E] (FIG. 7)     -   SEQ ID NO. 25—pABDP010 [complementary copy of         CZ28-bstar+UBQ10::NPTII::E9/LPAG1d4::bstar::NOST] (FIG. 8)     -   SEQ ID NO. 26—pABDP04 [complementary copy of         CZ28-bstar+UBQ10::NPTII::E9/LPAG1d4::bstar::NOST] (FIG. 9)

Sequences follow below. 

1.-102. (canceled)
 103. A method for obtaining wood pulp, comprising (a) introducing into a plant cell of a woody plant a construct comprising (i) a promoter having the sequence of any one of SEQ ID NOs. 4 or 16 operably linked to (ii) a desired nucleic acid encoding an E73G barnase mutant that comprises the sequence of SEQ ID NO. 5 or which comprises a nucleotide sequence that encodes the amino acid sequence of SEQ ID NO. 9; (b) culturing said transformed plant cell under conditions that promote growth of a plant; and (c) obtaining wood pulp from said plant.
 104. A construct, comprising (i) the sequence of either SEQ ID NOs. 4 or 16 operably linked to the sequence of SEQ ID NO: 5, or (ii) the sequence depicted in any one of SEQ ID NOs. 15, 20, or
 21. 105. A transgenic plant, comprising the construct of claim
 104. 106. A transgenic plant, comprising a construct that comprises a polynucleotide selected from any one of SEQ ID NO: 4 or 16 operably linked to a desired nucleic acid that comprises the sequence of SEQ ID NO. 5 or which encodes the amino acid sequence of SEQ ID NO.
 9. 107. A method for producing a transgenic plant, comprising (a) transforming a plant cell with a construct that comprises at least one polynucleotide having the sequence of any one of SEQ ID NOs. 4 or 16 operably linked to a desired nucleic acid, wherein said polynucleotide regulates the activity of said desired nucleic acid that has the sequence of SEQ ID NO. 5 or which encodes the amino acid sequence of SEQ ID NO. 5; (b) culturing said transformed plant cell under conditions that promote growth of a plant, wherein said plant is a transgenic plant that exhibits a phenotype that is different from a plant of the same species that does not contain said construct.
 108. A construct comprising a polynucleotide selected from any one of SEQ ID NO. 4 or 16 operably linked to a desired nucleic acid that comprises the sequence of SEQ ID NO. 5 which encodes SEQ ID NO. 9, wherein said polynucleotide regulates the expression of said desired nucleic acid in a plant cell transformed with the construct.
 109. A hybrid progeny plant transformed with a construct of claim
 104. 110. The hybrid progeny plant of claim 109, wherein the hybrid progeny plant is obtained from the cross of pitch Pinus rigida with loblolly pine P. taeda.
 111. A construct, comprising Pinus radiata male cone (PrMC) promoter operably linked to a desired nucleic acid, wherein the PrMC promoter regulates the expression of the desired nucleic acid that encodes an E73G barnase mutant in a plant cell transformed with the construct and wherein the E73G barnase mutant is capable of disrupting reproductive development of at least one of a male reproductive structure in a plant.
 112. The construct of claim 111, wherein the nucleic acid encoding the E73G barnase mutant comprises the sequence of SEQ ID NO.
 5. 113. The construct of claim 111, wherein the desired nucleic acid encodes the protein of SEQ ID NO.
 9. 114. The construct of claim 111, wherein the PrMC promoter/E73G barnase mutant construct comprises the sequence of SEQ ID NO.
 15. 115. A method for producing a transgenic plant, comprising (a) transforming a plant cell with a construct that comprises (i) a functional promoter having the sequence of SEQ ID NO. 4 or SEQ ID NO. 16 operably linked to (ii) an E73G mutant barnase-encoding polynucleotide; and (b) culturing the transformed plant cell under conditions that promote growth of a plant, wherein said plant is a transgenic plant that exhibits a phenotype that is different from a plant of the same species that has not been transformed with the construct.
 116. A method for producing a transgenic plant, comprising (a) transforming a plant cell with a construct that comprises (i) a functional PrMC promoter operably linked to (ii) a polynucleotide that comprises the sequence of SEQ ID NO. 5; and (b) culturing the transformed plant cell under conditions that promote growth of a plant, wherein said plant is a transgenic plant that exhibits a phenotype that is different from a plant of the same species that has not been transformed with the construct.
 117. A method for producing a transgenic plant, comprising (a) transforming a plant cell with a construct that comprises the sequence of any one of SEQ ID NOs. 15, 20, or 21; and (b) culturing the transformed plant cell under conditions that promote growth of a plant, wherein said plant is a transgenic plant that exhibits a phenotype that is different from a plant of the same species that has not been transformed with the construct. 